{
  "fields": [{"type":"int","id":"_id"},{"info":{"notes":"","type_override":"","label":"Year pregnancy ended"},"type":"numeric","id":"Year"},{"info":{"notes":"","type_override":"","label":"9 digit geography codes for Health Board of Residence in Scotland"},"type":"text","id":"HBR"},{"info":{"notes":"","type_override":"","label":"EUROCAT congenital condition group"},"type":"text","id":"ConditionGroup"},{"info":{"notes":"","type_override":"","label":"Number of births with associated congenital condition"},"type":"numeric","id":"Total"},{"info":{"notes":"","type_override":"","label":"Qualifier for Total"},"type":"text","id":"TotalQF"},{"info":{"notes":"","type_override":"","label":"Total Birth Population"},"type":"numeric","id":"TotalBirthPopulation"},{"info":{"notes":"","type_override":"","label":"Total Birth Prevalence (TBP) with associated congenital condition"},"type":"numeric","id":"TBP"},{"info":{"notes":"","type_override":"","label":"Qualifier for TBP"},"type":"text","id":"TBPQF"}],
  "records": [
    [1,2020,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",114,"",3060,372.5,""],
    [2,2020,"Ayrshire and Arran","Nervous system conditions",14,"",3060,45.8,""],
    [4,2020,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3060,0,""],
    [5,2020,"Ayrshire and Arran","Congenital heart diseases (CHD)",33,"",3060,107.8,""],
    [7,2020,"Ayrshire and Arran","Oro-facial clefts",6,"",3060,19.6,""],
    [8,2020,"Ayrshire and Arran","Gastro-intestinal conditions",9,"",3060,29.4,""],
    [9,2020,"Ayrshire and Arran","Abdominal wall defects",0,"",3060,0,""],
    [10,2020,"Ayrshire and Arran","Kidney and urinary tract conditions",20,"",3060,65.4,""],
    [11,2020,"Ayrshire and Arran","Genital conditions",7,"",3060,22.9,""],
    [12,2020,"Ayrshire and Arran","Limb conditions",19,"",3060,62.1,""],
    [14,2020,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",3060,52.3,""],
    [15,2020,"Borders","All major congenital conditions registerable by EUROCAT",11,"",806,136.5,""],
    [17,2020,"Borders","Eye conditions",0,"",806,0,""],
    [18,2020,"Borders","Ear, face and neck conditions",0,"",806,0,""],
    [20,2020,"Borders","Respiratory conditions",0,"",806,0,""],
    [23,2020,"Borders","Abdominal wall defects",0,"",806,0,""],
    [25,2020,"Borders","Genital conditions",0,"",806,0,""],
    [29,2020,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",26,"",1149,226.3,""],
    [31,2020,"Dumfries and Galloway","Eye conditions",0,"",1149,0,""],
    [32,2020,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1149,0,""],
    [33,2020,"Dumfries and Galloway","Congenital heart diseases (CHD)",13,"",1149,113.1,""],
    [37,2020,"Dumfries and Galloway","Abdominal wall defects",0,"",1149,0,""],
    [40,2020,"Dumfries and Galloway","Limb conditions",0,"",1149,0,""],
    [41,2020,"Dumfries and Galloway","Other conditions/syndromes",0,"",1149,0,""],
    [43,2020,"Fife","All major congenital conditions registerable by EUROCAT",64,"",3161,202.5,""],
    [44,2020,"Fife","Nervous system conditions",7,"",3161,22.1,""],
    [45,2020,"Fife","Eye conditions",0,"",3161,0,""],
    [46,2020,"Fife","Ear, face and neck conditions",0,"",3161,0,""],
    [47,2020,"Fife","Congenital heart diseases (CHD)",16,"",3161,50.6,""],
    [48,2020,"Fife","Respiratory conditions",0,"",3161,0,""],
    [49,2020,"Fife","Oro-facial clefts",8,"",3161,25.3,""],
    [52,2020,"Fife","Kidney and urinary tract conditions",5,"",3161,15.8,""],
    [53,2020,"Fife","Genital conditions",6,"",3161,19,""],
    [55,2020,"Fife","Other conditions/syndromes",0,"",3161,0,""],
    [56,2020,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",18,"",3161,56.9,""],
    [57,2020,"Forth Valley","All major congenital conditions registerable by EUROCAT",94,"",2619,358.9,""],
    [58,2020,"Forth Valley","Nervous system conditions",9,"",2619,34.4,""],
    [60,2020,"Forth Valley","Ear, face and neck conditions",0,"",2619,0,""],
    [61,2020,"Forth Valley","Congenital heart diseases (CHD)",22,"",2619,84,""],
    [64,2020,"Forth Valley","Gastro-intestinal conditions",9,"",2619,34.4,""],
    [65,2020,"Forth Valley","Abdominal wall defects",0,"",2619,0,""],
    [66,2020,"Forth Valley","Kidney and urinary tract conditions",7,"",2619,26.7,""],
    [67,2020,"Forth Valley","Genital conditions",20,"",2619,76.4,""],
    [68,2020,"Forth Valley","Limb conditions",9,"",2619,34.4,""],
    [70,2020,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",12,"",2619,45.8,""],
    [71,2020,"Grampian","All major congenital conditions registerable by EUROCAT",132,"",5199,253.9,""],
    [72,2020,"Grampian","Nervous system conditions",19,"",5199,36.5,""],
    [73,2020,"Grampian","Eye conditions",6,"",5199,11.5,""],
    [74,2020,"Grampian","Ear, face and neck conditions",0,"",5199,0,""],
    [75,2020,"Grampian","Congenital heart diseases (CHD)",26,"",5199,50,""],
    [76,2020,"Grampian","Respiratory conditions",5,"",5199,9.6,""],
    [77,2020,"Grampian","Oro-facial clefts",7,"",5199,13.5,""],
    [78,2020,"Grampian","Gastro-intestinal conditions",16,"",5199,30.8,""],
    [80,2020,"Grampian","Kidney and urinary tract conditions",10,"",5199,19.2,""],
    [81,2020,"Grampian","Genital conditions",14,"",5199,26.9,""],
    [82,2020,"Grampian","Limb conditions",14,"",5199,26.9,""],
    [83,2020,"Grampian","Other conditions/syndromes",9,"",5199,17.3,""],
    [84,2020,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",34,"",5199,65.4,""],
    [85,2020,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",296,"",10856,272.7,""],
    [86,2020,"Greater Glasgow and Clyde","Nervous system conditions",28,"",10856,25.8,""],
    [87,2020,"Greater Glasgow and Clyde","Eye conditions",5,"",10856,4.6,""],
    [89,2020,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",91,"",10856,83.8,""],
    [91,2020,"Greater Glasgow and Clyde","Oro-facial clefts",12,"",10856,11.1,""],
    [92,2020,"Greater Glasgow and Clyde","Gastro-intestinal conditions",31,"",10856,28.6,""],
    [94,2020,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",32,"",10856,29.5,""],
    [95,2020,"Greater Glasgow and Clyde","Genital conditions",17,"",10856,15.7,""],
    [96,2020,"Greater Glasgow and Clyde","Limb conditions",20,"",10856,18.4,""],
    [97,2020,"Greater Glasgow and Clyde","Other conditions/syndromes",17,"",10856,15.7,""],
    [98,2020,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",74,"",10856,68.2,""],
    [99,2020,"Highland","All major congenital conditions registerable by EUROCAT",92,"",2462,373.7,""],
    [100,2020,"Highland","Nervous system conditions",10,"",2462,40.6,""],
    [102,2020,"Highland","Ear, face and neck conditions",0,"",2462,0,""],
    [103,2020,"Highland","Congenital heart diseases (CHD)",38,"",2462,154.3,""],
    [108,2020,"Highland","Kidney and urinary tract conditions",9,"",2462,36.6,""],
    [110,2020,"Highland","Limb conditions",5,"",2462,20.3,""],
    [111,2020,"Highland","Other conditions/syndromes",6,"",2462,24.4,""],
    [112,2020,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",17,"",2462,69,""],
    [113,2020,"Lanarkshire","All major congenital conditions registerable by EUROCAT",277,"",6241,443.8,""],
    [114,2020,"Lanarkshire","Nervous system conditions",18,"",6241,28.8,""],
    [117,2020,"Lanarkshire","Congenital heart diseases (CHD)",58,"",6241,92.9,""],
    [119,2020,"Lanarkshire","Oro-facial clefts",11,"",6241,17.6,""],
    [120,2020,"Lanarkshire","Gastro-intestinal conditions",17,"",6241,27.2,""],
    [122,2020,"Lanarkshire","Kidney and urinary tract conditions",30,"",6241,48.1,""],
    [123,2020,"Lanarkshire","Genital conditions",22,"",6241,35.3,""],
    [124,2020,"Lanarkshire","Limb conditions",93,"",6241,149,""],
    [125,2020,"Lanarkshire","Other conditions/syndromes",6,"",6241,9.6,""],
    [126,2020,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",37,"",6241,59.3,""],
    [127,2020,"Lothian","All major congenital conditions registerable by EUROCAT",217,"",8246,263.2,""],
    [128,2020,"Lothian","Nervous system conditions",18,"",8246,21.8,""],
    [130,2020,"Lothian","Ear, face and neck conditions",0,"",8246,0,""],
    [131,2020,"Lothian","Congenital heart diseases (CHD)",48,"",8246,58.2,""],
    [133,2020,"Lothian","Oro-facial clefts",10,"",8246,12.1,""],
    [134,2020,"Lothian","Gastro-intestinal conditions",19,"",8246,23,""],
    [135,2020,"Lothian","Abdominal wall defects",10,"",8246,12.1,""],
    [136,2020,"Lothian","Kidney and urinary tract conditions",19,"",8246,23,""],
    [137,2020,"Lothian","Genital conditions",28,"",8246,34,""],
    [138,2020,"Lothian","Limb conditions",28,"",8246,34,""],
    [139,2020,"Lothian","Other conditions/syndromes",7,"",8246,8.5,""],
    [140,2020,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",41,"",8246,49.7,""],
    [142,2020,"Orkney","Nervous system conditions",0,"",180,0,""],
    [143,2020,"Orkney","Eye conditions",0,"",180,0,""],
    [144,2020,"Orkney","Ear, face and neck conditions",0,"",180,0,""],
    [146,2020,"Orkney","Respiratory conditions",0,"",180,0,""],
    [147,2020,"Orkney","Oro-facial clefts",0,"",180,0,""],
    [148,2020,"Orkney","Gastro-intestinal conditions",0,"",180,0,""],
    [149,2020,"Orkney","Abdominal wall defects",0,"",180,0,""],
    [150,2020,"Orkney","Kidney and urinary tract conditions",0,"",180,0,""],
    [151,2020,"Orkney","Genital conditions",0,"",180,0,""],
    [152,2020,"Orkney","Limb conditions",0,"",180,0,""],
    [153,2020,"Orkney","Other conditions/syndromes",0,"",180,0,""],
    [154,2020,"Orkney","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",180,0,""],
    [155,2020,"Shetland","All major congenital conditions registerable by EUROCAT",6,"",181,331.5,""],
    [156,2020,"Shetland","Nervous system conditions",0,"",181,0,""],
    [157,2020,"Shetland","Eye conditions",0,"",181,0,""],
    [161,2020,"Shetland","Oro-facial clefts",0,"",181,0,""],
    [165,2020,"Shetland","Genital conditions",0,"",181,0,""],
    [167,2020,"Shetland","Other conditions/syndromes",0,"",181,0,""],
    [169,2020,"Tayside","All major congenital conditions registerable by EUROCAT",59,"",3383,174.4,""],
    [170,2020,"Tayside","Nervous system conditions",5,"",3383,14.8,""],
    [172,2020,"Tayside","Ear, face and neck conditions",0,"",3383,0,""],
    [173,2020,"Tayside","Congenital heart diseases (CHD)",16,"",3383,47.3,""],
    [175,2020,"Tayside","Oro-facial clefts",6,"",3383,17.7,""],
    [176,2020,"Tayside","Gastro-intestinal conditions",5,"",3383,14.8,""],
    [180,2020,"Tayside","Limb conditions",7,"",3383,20.7,""],
    [182,2020,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",9,"",3383,26.6,""],
    [183,2020,"Total","All major congenital conditions registerable by EUROCAT",1396,"",47867,291.6,""],
    [184,2020,"Total","Nervous system conditions",133,"",47867,27.8,""],
    [185,2020,"Total","Eye conditions",21,"",47867,4.4,""],
    [186,2020,"Total","Ear, face and neck conditions",5,"",47867,1,""],
    [187,2020,"Total","Congenital heart diseases (CHD)",367,"",47867,76.7,""],
    [188,2020,"Total","Respiratory conditions",22,"",47867,4.6,""],
    [189,2020,"Total","Oro-facial clefts",72,"",47867,15,""],
    [190,2020,"Total","Gastro-intestinal conditions",116,"",47867,24.2,""],
    [191,2020,"Total","Abdominal wall defects",25,"",47867,5.2,""],
    [192,2020,"Total","Kidney and urinary tract conditions",142,"",47867,29.7,""],
    [193,2020,"Total","Genital conditions",120,"",47867,25.1,""],
    [194,2020,"Total","Limb conditions",204,"",47867,42.6,""],
    [195,2020,"Total","Other conditions/syndromes",53,"",47867,11.1,""],
    [196,2020,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",268,"",47867,56,""],
    [197,2020,"Western Isles","All major congenital conditions registerable by EUROCAT",5,"",186,268.8,""],
    [199,2020,"Western Isles","Eye conditions",0,"",186,0,""],
    [200,2020,"Western Isles","Ear, face and neck conditions",0,"",186,0,""],
    [202,2020,"Western Isles","Respiratory conditions",0,"",186,0,""],
    [204,2020,"Western Isles","Gastro-intestinal conditions",0,"",186,0,""],
    [205,2020,"Western Isles","Abdominal wall defects",0,"",186,0,""],
    [208,2020,"Western Isles","Limb conditions",0,"",186,0,""],
    [209,2020,"Western Isles","Other conditions/syndromes",0,"",186,0,""],
    [211,2019,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",129,"",3133,411.7,""],
    [212,2019,"Ayrshire and Arran","Nervous system conditions",9,"",3133,28.7,""],
    [214,2019,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3133,0,""],
    [215,2019,"Ayrshire and Arran","Congenital heart diseases (CHD)",36,"",3133,114.9,""],
    [218,2019,"Ayrshire and Arran","Gastro-intestinal conditions",7,"",3133,22.3,""],
    [220,2019,"Ayrshire and Arran","Kidney and urinary tract conditions",15,"",3133,47.9,""],
    [221,2019,"Ayrshire and Arran","Genital conditions",18,"",3133,57.5,""],
    [222,2019,"Ayrshire and Arran","Limb conditions",16,"",3133,51.1,""],
    [223,2019,"Ayrshire and Arran","Other conditions/syndromes",8,"",3133,25.5,""],
    [224,2019,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",14,"",3133,44.7,""],
    [225,2019,"Borders","All major congenital conditions registerable by EUROCAT",17,"",863,197,""],
    [227,2019,"Borders","Eye conditions",0,"",863,0,""],
    [228,2019,"Borders","Ear, face and neck conditions",0,"",863,0,""],
    [230,2019,"Borders","Respiratory conditions",0,"",863,0,""],
    [234,2019,"Borders","Kidney and urinary tract conditions",0,"",863,0,""],
    [239,2019,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",37,"",1135,326,""],
    [240,2019,"Dumfries and Galloway","Nervous system conditions",8,"",1135,70.5,""],
    [242,2019,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1135,0,""],
    [243,2019,"Dumfries and Galloway","Congenital heart diseases (CHD)",8,"",1135,70.5,""],
    [247,2019,"Dumfries and Galloway","Abdominal wall defects",0,"",1135,0,""],
    [249,2019,"Dumfries and Galloway","Genital conditions",0,"",1135,0,""],
    [252,2019,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",9,"",1135,79.3,""],
    [253,2019,"Fife","All major congenital conditions registerable by EUROCAT",73,"",3289,222,""],
    [254,2019,"Fife","Nervous system conditions",10,"",3289,30.4,""],
    [257,2019,"Fife","Congenital heart diseases (CHD)",25,"",3289,76,""],
    [258,2019,"Fife","Respiratory conditions",0,"",3289,0,""],
    [259,2019,"Fife","Oro-facial clefts",8,"",3289,24.3,""],
    [260,2019,"Fife","Gastro-intestinal conditions",7,"",3289,21.3,""],
    [262,2019,"Fife","Kidney and urinary tract conditions",6,"",3289,18.2,""],
    [264,2019,"Fife","Limb conditions",10,"",3289,30.4,""],
    [266,2019,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",3289,45.6,""],
    [267,2019,"Forth Valley","All major congenital conditions registerable by EUROCAT",85,"",2621,324.3,""],
    [270,2019,"Forth Valley","Ear, face and neck conditions",0,"",2621,0,""],
    [271,2019,"Forth Valley","Congenital heart diseases (CHD)",23,"",2621,87.8,""],
    [276,2019,"Forth Valley","Kidney and urinary tract conditions",8,"",2621,30.5,""],
    [277,2019,"Forth Valley","Genital conditions",16,"",2621,61,""],
    [278,2019,"Forth Valley","Limb conditions",16,"",2621,61,""],
    [280,2019,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",13,"",2621,49.6,""],
    [281,2019,"Grampian","All major congenital conditions registerable by EUROCAT",161,"",5488,293.4,""],
    [282,2019,"Grampian","Nervous system conditions",26,"",5488,47.4,""],
    [284,2019,"Grampian","Ear, face and neck conditions",0,"",5488,0,""],
    [285,2019,"Grampian","Congenital heart diseases (CHD)",38,"",5488,69.2,""],
    [287,2019,"Grampian","Oro-facial clefts",10,"",5488,18.2,""],
    [288,2019,"Grampian","Gastro-intestinal conditions",9,"",5488,16.4,""],
    [289,2019,"Grampian","Abdominal wall defects",5,"",5488,9.1,""],
    [290,2019,"Grampian","Kidney and urinary tract conditions",15,"",5488,27.3,""],
    [291,2019,"Grampian","Genital conditions",11,"",5488,20,""],
    [292,2019,"Grampian","Limb conditions",19,"",5488,34.6,""],
    [293,2019,"Grampian","Other conditions/syndromes",9,"",5488,16.4,""],
    [294,2019,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",27,"",5488,49.2,""],
    [295,2019,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",317,"",11272,281.2,""],
    [296,2019,"Greater Glasgow and Clyde","Nervous system conditions",47,"",11272,41.7,""],
    [297,2019,"Greater Glasgow and Clyde","Eye conditions",6,"",11272,5.3,""],
    [299,2019,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",78,"",11272,69.2,""],
    [300,2019,"Greater Glasgow and Clyde","Respiratory conditions",6,"",11272,5.3,""],
    [301,2019,"Greater Glasgow and Clyde","Oro-facial clefts",16,"",11272,14.2,""],
    [302,2019,"Greater Glasgow and Clyde","Gastro-intestinal conditions",37,"",11272,32.8,""],
    [304,2019,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",31,"",11272,27.5,""],
    [305,2019,"Greater Glasgow and Clyde","Genital conditions",19,"",11272,16.9,""],
    [306,2019,"Greater Glasgow and Clyde","Limb conditions",30,"",11272,26.6,""],
    [307,2019,"Greater Glasgow and Clyde","Other conditions/syndromes",16,"",11272,14.2,""],
    [308,2019,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",68,"",11272,60.3,""],
    [309,2019,"Highland","All major congenital conditions registerable by EUROCAT",119,"",2581,461.1,""],
    [310,2019,"Highland","Nervous system conditions",15,"",2581,58.1,""],
    [311,2019,"Highland","Eye conditions",0,"",2581,0,""],
    [313,2019,"Highland","Congenital heart diseases (CHD)",59,"",2581,228.6,""],
    [316,2019,"Highland","Gastro-intestinal conditions",7,"",2581,27.1,""],
    [317,2019,"Highland","Abdominal wall defects",0,"",2581,0,""],
    [318,2019,"Highland","Kidney and urinary tract conditions",10,"",2581,38.7,""],
    [319,2019,"Highland","Genital conditions",8,"",2581,31,""],
    [320,2019,"Highland","Limb conditions",14,"",2581,54.2,""],
    [321,2019,"Highland","Other conditions/syndromes",6,"",2581,23.2,""],
    [322,2019,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",12,"",2581,46.5,""],
    [323,2019,"Lanarkshire","All major congenital conditions registerable by EUROCAT",251,"",6525,384.7,""],
    [324,2019,"Lanarkshire","Nervous system conditions",17,"",6525,26.1,""],
    [327,2019,"Lanarkshire","Congenital heart diseases (CHD)",39,"",6525,59.8,""],
    [330,2019,"Lanarkshire","Gastro-intestinal conditions",14,"",6525,21.5,""],
    [332,2019,"Lanarkshire","Kidney and urinary tract conditions",26,"",6525,39.8,""],
    [333,2019,"Lanarkshire","Genital conditions",24,"",6525,36.8,""],
    [334,2019,"Lanarkshire","Limb conditions",92,"",6525,141,""],
    [335,2019,"Lanarkshire","Other conditions/syndromes",6,"",6525,9.2,""],
    [336,2019,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",28,"",6525,42.9,""],
    [337,2019,"Lothian","All major congenital conditions registerable by EUROCAT",265,"",8471,312.8,""],
    [338,2019,"Lothian","Nervous system conditions",29,"",8471,34.2,""],
    [339,2019,"Lothian","Eye conditions",8,"",8471,9.4,""],
    [340,2019,"Lothian","Ear, face and neck conditions",0,"",8471,0,""],
    [341,2019,"Lothian","Congenital heart diseases (CHD)",42,"",8471,49.6,""],
    [343,2019,"Lothian","Oro-facial clefts",12,"",8471,14.2,""],
    [344,2019,"Lothian","Gastro-intestinal conditions",15,"",8471,17.7,""],
    [345,2019,"Lothian","Abdominal wall defects",6,"",8471,7.1,""],
    [346,2019,"Lothian","Kidney and urinary tract conditions",27,"",8471,31.9,""],
    [347,2019,"Lothian","Genital conditions",40,"",8471,47.2,""],
    [348,2019,"Lothian","Limb conditions",46,"",8471,54.3,""],
    [349,2019,"Lothian","Other conditions/syndromes",5,"",8471,5.9,""],
    [350,2019,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",45,"",8471,53.1,""],
    [353,2019,"Orkney","Eye conditions",0,"",181,0,""],
    [354,2019,"Orkney","Ear, face and neck conditions",0,"",181,0,""],
    [356,2019,"Orkney","Respiratory conditions",0,"",181,0,""],
    [358,2019,"Orkney","Gastro-intestinal conditions",0,"",181,0,""],
    [359,2019,"Orkney","Abdominal wall defects",0,"",181,0,""],
    [360,2019,"Orkney","Kidney and urinary tract conditions",0,"",181,0,""],
    [361,2019,"Orkney","Genital conditions",0,"",181,0,""],
    [362,2019,"Orkney","Limb conditions",0,"",181,0,""],
    [363,2019,"Orkney","Other conditions/syndromes",0,"",181,0,""],
    [364,2019,"Orkney","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",181,0,""],
    [365,2019,"Shetland","All major congenital conditions registerable by EUROCAT",6,"",198,303,""],
    [367,2019,"Shetland","Eye conditions",0,"",198,0,""],
    [368,2019,"Shetland","Ear, face and neck conditions",0,"",198,0,""],
    [370,2019,"Shetland","Respiratory conditions",0,"",198,0,""],
    [371,2019,"Shetland","Oro-facial clefts",0,"",198,0,""],
    [372,2019,"Shetland","Gastro-intestinal conditions",0,"",198,0,""],
    [373,2019,"Shetland","Abdominal wall defects",0,"",198,0,""],
    [374,2019,"Shetland","Kidney and urinary tract conditions",0,"",198,0,""],
    [375,2019,"Shetland","Genital conditions",0,"",198,0,""],
    [376,2019,"Shetland","Limb conditions",0,"",198,0,""],
    [377,2019,"Shetland","Other conditions/syndromes",0,"",198,0,""],
    [379,2019,"Tayside","All major congenital conditions registerable by EUROCAT",75,"",3554,211,""],
    [380,2019,"Tayside","Nervous system conditions",15,"",3554,42.2,""],
    [383,2019,"Tayside","Congenital heart diseases (CHD)",18,"",3554,50.6,""],
    [386,2019,"Tayside","Gastro-intestinal conditions",13,"",3554,36.6,""],
    [389,2019,"Tayside","Genital conditions",10,"",3554,28.1,""],
    [390,2019,"Tayside","Limb conditions",9,"",3554,25.3,""],
    [391,2019,"Tayside","Other conditions/syndromes",6,"",3554,16.9,""],
    [392,2019,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",14,"",3554,39.4,""],
    [393,2019,"Total","All major congenital conditions registerable by EUROCAT",1550,"",49646,312.2,""],
    [394,2019,"Total","Nervous system conditions",183,"",49646,36.9,""],
    [395,2019,"Total","Eye conditions",28,"",49646,5.6,""],
    [396,2019,"Total","Ear, face and neck conditions",8,"",49646,1.6,""],
    [397,2019,"Total","Congenital heart diseases (CHD)",375,"",49646,75.5,""],
    [398,2019,"Total","Respiratory conditions",25,"",49646,5,""],
    [399,2019,"Total","Oro-facial clefts",68,"",49646,13.7,""],
    [400,2019,"Total","Gastro-intestinal conditions",115,"",49646,23.2,""],
    [401,2019,"Total","Abdominal wall defects",26,"",49646,5.2,""],
    [402,2019,"Total","Kidney and urinary tract conditions",148,"",49646,29.8,""],
    [403,2019,"Total","Genital conditions",151,"",49646,30.4,""],
    [404,2019,"Total","Limb conditions",257,"",49646,51.8,""],
    [405,2019,"Total","Other conditions/syndromes",67,"",49646,13.5,""],
    [406,2019,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",250,"",49646,50.4,""],
    [407,2019,"Western Isles","All major congenital conditions registerable by EUROCAT",9,"",201,447.8,""],
    [408,2019,"Western Isles","Nervous system conditions",0,"",201,0,""],
    [409,2019,"Western Isles","Eye conditions",0,"",201,0,""],
    [410,2019,"Western Isles","Ear, face and neck conditions",0,"",201,0,""],
    [412,2019,"Western Isles","Respiratory conditions",0,"",201,0,""],
    [413,2019,"Western Isles","Oro-facial clefts",0,"",201,0,""],
    [414,2019,"Western Isles","Gastro-intestinal conditions",0,"",201,0,""],
    [415,2019,"Western Isles","Abdominal wall defects",0,"",201,0,""],
    [419,2019,"Western Isles","Other conditions/syndromes",0,"",201,0,""],
    [420,2019,"Western Isles","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",201,0,""],
    [421,2018,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",130,"",3218,404,""],
    [422,2018,"Ayrshire and Arran","Nervous system conditions",9,"",3218,28,""],
    [423,2018,"Ayrshire and Arran","Eye conditions",5,"",3218,15.5,""],
    [424,2018,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3218,0,""],
    [425,2018,"Ayrshire and Arran","Congenital heart diseases (CHD)",40,"",3218,124.3,""],
    [428,2018,"Ayrshire and Arran","Gastro-intestinal conditions",18,"",3218,55.9,""],
    [430,2018,"Ayrshire and Arran","Kidney and urinary tract conditions",17,"",3218,52.8,""],
    [431,2018,"Ayrshire and Arran","Genital conditions",13,"",3218,40.4,""],
    [432,2018,"Ayrshire and Arran","Limb conditions",15,"",3218,46.6,""],
    [433,2018,"Ayrshire and Arran","Other conditions/syndromes",7,"",3218,21.8,""],
    [434,2018,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",18,"",3218,55.9,""],
    [435,2018,"Borders","All major congenital conditions registerable by EUROCAT",19,"",916,207.4,""],
    [438,2018,"Borders","Ear, face and neck conditions",0,"",916,0,""],
    [440,2018,"Borders","Respiratory conditions",0,"",916,0,""],
    [443,2018,"Borders","Abdominal wall defects",0,"",916,0,""],
    [448,2018,"Borders","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",916,0,""],
    [449,2018,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",33,"",1189,277.5,""],
    [453,2018,"Dumfries and Galloway","Congenital heart diseases (CHD)",8,"",1189,67.3,""],
    [456,2018,"Dumfries and Galloway","Gastro-intestinal conditions",6,"",1189,50.5,""],
    [462,2018,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",6,"",1189,50.5,""],
    [463,2018,"Fife","All major congenital conditions registerable by EUROCAT",67,"",3540,189.3,""],
    [464,2018,"Fife","Nervous system conditions",9,"",3540,25.4,""],
    [467,2018,"Fife","Congenital heart diseases (CHD)",23,"",3540,65,""],
    [469,2018,"Fife","Oro-facial clefts",6,"",3540,16.9,""],
    [470,2018,"Fife","Gastro-intestinal conditions",8,"",3540,22.6,""],
    [474,2018,"Fife","Limb conditions",5,"",3540,14.1,""],
    [476,2018,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",20,"",3540,56.5,""],
    [477,2018,"Forth Valley","All major congenital conditions registerable by EUROCAT",103,"",2716,379.2,""],
    [478,2018,"Forth Valley","Nervous system conditions",8,"",2716,29.5,""],
    [480,2018,"Forth Valley","Ear, face and neck conditions",0,"",2716,0,""],
    [481,2018,"Forth Valley","Congenital heart diseases (CHD)",30,"",2716,110.5,""],
    [482,2018,"Forth Valley","Respiratory conditions",0,"",2716,0,""],
    [483,2018,"Forth Valley","Oro-facial clefts",5,"",2716,18.4,""],
    [484,2018,"Forth Valley","Gastro-intestinal conditions",7,"",2716,25.8,""],
    [486,2018,"Forth Valley","Kidney and urinary tract conditions",13,"",2716,47.9,""],
    [487,2018,"Forth Valley","Genital conditions",13,"",2716,47.9,""],
    [488,2018,"Forth Valley","Limb conditions",9,"",2716,33.1,""],
    [490,2018,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",17,"",2716,62.6,""],
    [491,2018,"Grampian","All major congenital conditions registerable by EUROCAT",164,"",5852,280.2,""],
    [492,2018,"Grampian","Nervous system conditions",18,"",5852,30.8,""],
    [495,2018,"Grampian","Congenital heart diseases (CHD)",42,"",5852,71.8,""],
    [497,2018,"Grampian","Oro-facial clefts",6,"",5852,10.3,""],
    [498,2018,"Grampian","Gastro-intestinal conditions",9,"",5852,15.4,""],
    [499,2018,"Grampian","Abdominal wall defects",5,"",5852,8.5,""],
    [500,2018,"Grampian","Kidney and urinary tract conditions",14,"",5852,23.9,""],
    [501,2018,"Grampian","Genital conditions",19,"",5852,32.5,""],
    [502,2018,"Grampian","Limb conditions",25,"",5852,42.7,""],
    [503,2018,"Grampian","Other conditions/syndromes",7,"",5852,12,""],
    [504,2018,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",29,"",5852,49.6,""],
    [505,2018,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",248,"",11701,211.9,""],
    [506,2018,"Greater Glasgow and Clyde","Nervous system conditions",38,"",11701,32.5,""],
    [507,2018,"Greater Glasgow and Clyde","Eye conditions",7,"",11701,6,""],
    [509,2018,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",63,"",11701,53.8,""],
    [510,2018,"Greater Glasgow and Clyde","Respiratory conditions",5,"",11701,4.3,""],
    [511,2018,"Greater Glasgow and Clyde","Oro-facial clefts",13,"",11701,11.1,""],
    [512,2018,"Greater Glasgow and Clyde","Gastro-intestinal conditions",16,"",11701,13.7,""],
    [513,2018,"Greater Glasgow and Clyde","Abdominal wall defects",5,"",11701,4.3,""],
    [514,2018,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",26,"",11701,22.2,""],
    [515,2018,"Greater Glasgow and Clyde","Genital conditions",16,"",11701,13.7,""],
    [516,2018,"Greater Glasgow and Clyde","Limb conditions",14,"",11701,12,""],
    [517,2018,"Greater Glasgow and Clyde","Other conditions/syndromes",11,"",11701,9.4,""],
    [518,2018,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",40,"",11701,34.2,""],
    [519,2018,"Highland","All major congenital conditions registerable by EUROCAT",106,"",2653,399.5,""],
    [520,2018,"Highland","Nervous system conditions",9,"",2653,33.9,""],
    [522,2018,"Highland","Ear, face and neck conditions",0,"",2653,0,""],
    [523,2018,"Highland","Congenital heart diseases (CHD)",54,"",2653,203.5,""],
    [525,2018,"Highland","Oro-facial clefts",6,"",2653,22.6,""],
    [526,2018,"Highland","Gastro-intestinal conditions",6,"",2653,22.6,""],
    [527,2018,"Highland","Abdominal wall defects",0,"",2653,0,""],
    [528,2018,"Highland","Kidney and urinary tract conditions",7,"",2653,26.4,""],
    [529,2018,"Highland","Genital conditions",12,"",2653,45.2,""],
    [530,2018,"Highland","Limb conditions",12,"",2653,45.2,""],
    [531,2018,"Highland","Other conditions/syndromes",5,"",2653,18.8,""],
    [532,2018,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",2653,60.3,""],
    [533,2018,"Lanarkshire","All major congenital conditions registerable by EUROCAT",192,"",6529,294.1,""],
    [534,2018,"Lanarkshire","Nervous system conditions",20,"",6529,30.6,""],
    [536,2018,"Lanarkshire","Ear, face and neck conditions",0,"",6529,0,""],
    [537,2018,"Lanarkshire","Congenital heart diseases (CHD)",35,"",6529,53.6,""],
    [539,2018,"Lanarkshire","Oro-facial clefts",9,"",6529,13.8,""],
    [540,2018,"Lanarkshire","Gastro-intestinal conditions",16,"",6529,24.5,""],
    [541,2018,"Lanarkshire","Abdominal wall defects",5,"",6529,7.7,""],
    [542,2018,"Lanarkshire","Kidney and urinary tract conditions",9,"",6529,13.8,""],
    [543,2018,"Lanarkshire","Genital conditions",27,"",6529,41.4,""],
    [544,2018,"Lanarkshire","Limb conditions",32,"",6529,49,""],
    [545,2018,"Lanarkshire","Other conditions/syndromes",8,"",6529,12.3,""],
    [546,2018,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",41,"",6529,62.8,""],
    [547,2018,"Lothian","All major congenital conditions registerable by EUROCAT",336,"",8792,382.2,""],
    [548,2018,"Lothian","Nervous system conditions",27,"",8792,30.7,""],
    [549,2018,"Lothian","Eye conditions",6,"",8792,6.8,""],
    [551,2018,"Lothian","Congenital heart diseases (CHD)",66,"",8792,75.1,""],
    [552,2018,"Lothian","Respiratory conditions",7,"",8792,8,""],
    [553,2018,"Lothian","Oro-facial clefts",14,"",8792,15.9,""],
    [554,2018,"Lothian","Gastro-intestinal conditions",18,"",8792,20.5,""],
    [555,2018,"Lothian","Abdominal wall defects",5,"",8792,5.7,""],
    [556,2018,"Lothian","Kidney and urinary tract conditions",28,"",8792,31.8,""],
    [557,2018,"Lothian","Genital conditions",55,"",8792,62.6,""],
    [558,2018,"Lothian","Limb conditions",66,"",8792,75.1,""],
    [559,2018,"Lothian","Other conditions/syndromes",10,"",8792,11.4,""],
    [560,2018,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",59,"",8792,67.1,""],
    [562,2018,"Orkney","Nervous system conditions",0,"",175,0,""],
    [563,2018,"Orkney","Eye conditions",0,"",175,0,""],
    [564,2018,"Orkney","Ear, face and neck conditions",0,"",175,0,""],
    [565,2018,"Orkney","Congenital heart diseases (CHD)",0,"",175,0,""],
    [566,2018,"Orkney","Respiratory conditions",0,"",175,0,""],
    [567,2018,"Orkney","Oro-facial clefts",0,"",175,0,""],
    [568,2018,"Orkney","Gastro-intestinal conditions",0,"",175,0,""],
    [569,2018,"Orkney","Abdominal wall defects",0,"",175,0,""],
    [570,2018,"Orkney","Kidney and urinary tract conditions",0,"",175,0,""],
    [571,2018,"Orkney","Genital conditions",0,"",175,0,""],
    [572,2018,"Orkney","Limb conditions",0,"",175,0,""],
    [573,2018,"Orkney","Other conditions/syndromes",0,"",175,0,""],
    [575,2018,"Shetland","All major congenital conditions registerable by EUROCAT",5,"",219,228.3,""],
    [576,2018,"Shetland","Nervous system conditions",0,"",219,0,""],
    [578,2018,"Shetland","Ear, face and neck conditions",0,"",219,0,""],
    [580,2018,"Shetland","Respiratory conditions",0,"",219,0,""],
    [582,2018,"Shetland","Gastro-intestinal conditions",0,"",219,0,""],
    [583,2018,"Shetland","Abdominal wall defects",0,"",219,0,""],
    [584,2018,"Shetland","Kidney and urinary tract conditions",0,"",219,0,""],
    [585,2018,"Shetland","Genital conditions",0,"",219,0,""],
    [587,2018,"Shetland","Other conditions/syndromes",0,"",219,0,""],
    [589,2018,"Tayside","All major congenital conditions registerable by EUROCAT",84,"",3643,230.6,""],
    [590,2018,"Tayside","Nervous system conditions",11,"",3643,30.2,""],
    [593,2018,"Tayside","Congenital heart diseases (CHD)",15,"",3643,41.2,""],
    [595,2018,"Tayside","Oro-facial clefts",10,"",3643,27.4,""],
    [598,2018,"Tayside","Kidney and urinary tract conditions",7,"",3643,19.2,""],
    [599,2018,"Tayside","Genital conditions",15,"",3643,41.2,""],
    [600,2018,"Tayside","Limb conditions",5,"",3643,13.7,""],
    [602,2018,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",14,"",3643,38.4,""],
    [603,2018,"Total","All major congenital conditions registerable by EUROCAT",1495,"",51490,290.3,""],
    [604,2018,"Total","Nervous system conditions",154,"",51490,29.9,""],
    [605,2018,"Total","Eye conditions",35,"",51490,6.8,""],
    [606,2018,"Total","Ear, face and neck conditions",11,"",51490,2.1,""],
    [607,2018,"Total","Congenital heart diseases (CHD)",380,"",51490,73.8,""],
    [608,2018,"Total","Respiratory conditions",27,"",51490,5.2,""],
    [609,2018,"Total","Oro-facial clefts",75,"",51490,14.6,""],
    [610,2018,"Total","Gastro-intestinal conditions",112,"",51490,21.8,""],
    [611,2018,"Total","Abdominal wall defects",29,"",51490,5.6,""],
    [612,2018,"Total","Kidney and urinary tract conditions",129,"",51490,25.1,""],
    [613,2018,"Total","Genital conditions",181,"",51490,35.2,""],
    [614,2018,"Total","Limb conditions",189,"",51490,36.7,""],
    [615,2018,"Total","Other conditions/syndromes",60,"",51490,11.7,""],
    [616,2018,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",265,"",51490,51.5,""],
    [617,2018,"Western Isles","All major congenital conditions registerable by EUROCAT",5,"",198,252.5,""],
    [618,2018,"Western Isles","Nervous system conditions",0,"",198,0,""],
    [619,2018,"Western Isles","Eye conditions",0,"",198,0,""],
    [620,2018,"Western Isles","Ear, face and neck conditions",0,"",198,0,""],
    [622,2018,"Western Isles","Respiratory conditions",0,"",198,0,""],
    [623,2018,"Western Isles","Oro-facial clefts",0,"",198,0,""],
    [625,2018,"Western Isles","Abdominal wall defects",0,"",198,0,""],
    [629,2018,"Western Isles","Other conditions/syndromes",0,"",198,0,""],
    [631,2017,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",120,"",3314,362.1,""],
    [632,2017,"Ayrshire and Arran","Nervous system conditions",9,"",3314,27.2,""],
    [635,2017,"Ayrshire and Arran","Congenital heart diseases (CHD)",31,"",3314,93.5,""],
    [637,2017,"Ayrshire and Arran","Oro-facial clefts",5,"",3314,15.1,""],
    [638,2017,"Ayrshire and Arran","Gastro-intestinal conditions",11,"",3314,33.2,""],
    [640,2017,"Ayrshire and Arran","Kidney and urinary tract conditions",19,"",3314,57.3,""],
    [641,2017,"Ayrshire and Arran","Genital conditions",16,"",3314,48.3,""],
    [642,2017,"Ayrshire and Arran","Limb conditions",15,"",3314,45.3,""],
    [643,2017,"Ayrshire and Arran","Other conditions/syndromes",6,"",3314,18.1,""],
    [644,2017,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",11,"",3314,33.2,""],
    [645,2017,"Borders","All major congenital conditions registerable by EUROCAT",17,"",929,183,""],
    [646,2017,"Borders","Nervous system conditions",0,"",929,0,""],
    [647,2017,"Borders","Eye conditions",0,"",929,0,""],
    [648,2017,"Borders","Ear, face and neck conditions",0,"",929,0,""],
    [649,2017,"Borders","Congenital heart diseases (CHD)",7,"",929,75.3,""],
    [650,2017,"Borders","Respiratory conditions",0,"",929,0,""],
    [654,2017,"Borders","Kidney and urinary tract conditions",0,"",929,0,""],
    [659,2017,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",24,"",1246,192.6,""],
    [661,2017,"Dumfries and Galloway","Eye conditions",0,"",1246,0,""],
    [662,2017,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1246,0,""],
    [663,2017,"Dumfries and Galloway","Congenital heart diseases (CHD)",6,"",1246,48.2,""],
    [667,2017,"Dumfries and Galloway","Abdominal wall defects",0,"",1246,0,""],
    [669,2017,"Dumfries and Galloway","Genital conditions",0,"",1246,0,""],
    [670,2017,"Dumfries and Galloway","Limb conditions",0,"",1246,0,""],
    [673,2017,"Fife","All major congenital conditions registerable by EUROCAT",85,"",3482,244.1,""],
    [674,2017,"Fife","Nervous system conditions",14,"",3482,40.2,""],
    [676,2017,"Fife","Ear, face and neck conditions",0,"",3482,0,""],
    [677,2017,"Fife","Congenital heart diseases (CHD)",23,"",3482,66.1,""],
    [679,2017,"Fife","Oro-facial clefts",7,"",3482,20.1,""],
    [680,2017,"Fife","Gastro-intestinal conditions",6,"",3482,17.2,""],
    [682,2017,"Fife","Kidney and urinary tract conditions",9,"",3482,25.8,""],
    [683,2017,"Fife","Genital conditions",9,"",3482,25.8,""],
    [684,2017,"Fife","Limb conditions",5,"",3482,14.4,""],
    [685,2017,"Fife","Other conditions/syndromes",7,"",3482,20.1,""],
    [686,2017,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",20,"",3482,57.4,""],
    [687,2017,"Forth Valley","All major congenital conditions registerable by EUROCAT",98,"",2899,338,""],
    [688,2017,"Forth Valley","Nervous system conditions",13,"",2899,44.8,""],
    [690,2017,"Forth Valley","Ear, face and neck conditions",0,"",2899,0,""],
    [691,2017,"Forth Valley","Congenital heart diseases (CHD)",33,"",2899,113.8,""],
    [692,2017,"Forth Valley","Respiratory conditions",5,"",2899,17.2,""],
    [694,2017,"Forth Valley","Gastro-intestinal conditions",8,"",2899,27.6,""],
    [696,2017,"Forth Valley","Kidney and urinary tract conditions",12,"",2899,41.4,""],
    [697,2017,"Forth Valley","Genital conditions",10,"",2899,34.5,""],
    [698,2017,"Forth Valley","Limb conditions",9,"",2899,31,""],
    [699,2017,"Forth Valley","Other conditions/syndromes",7,"",2899,24.1,""],
    [700,2017,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",19,"",2899,65.5,""],
    [701,2017,"Grampian","All major congenital conditions registerable by EUROCAT",237,"",5953,398.1,""],
    [702,2017,"Grampian","Nervous system conditions",26,"",5953,43.7,""],
    [703,2017,"Grampian","Eye conditions",5,"",5953,8.4,""],
    [704,2017,"Grampian","Ear, face and neck conditions",0,"",5953,0,""],
    [705,2017,"Grampian","Congenital heart diseases (CHD)",62,"",5953,104.1,""],
    [707,2017,"Grampian","Oro-facial clefts",6,"",5953,10.1,""],
    [708,2017,"Grampian","Gastro-intestinal conditions",19,"",5953,31.9,""],
    [710,2017,"Grampian","Kidney and urinary tract conditions",23,"",5953,38.6,""],
    [711,2017,"Grampian","Genital conditions",30,"",5953,50.4,""],
    [712,2017,"Grampian","Limb conditions",43,"",5953,72.2,""],
    [713,2017,"Grampian","Other conditions/syndromes",9,"",5953,15.1,""],
    [714,2017,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",32,"",5953,53.8,""],
    [715,2017,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",427,"",12173,350.8,""],
    [716,2017,"Greater Glasgow and Clyde","Nervous system conditions",48,"",12173,39.4,""],
    [717,2017,"Greater Glasgow and Clyde","Eye conditions",15,"",12173,12.3,""],
    [719,2017,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",120,"",12173,98.6,""],
    [721,2017,"Greater Glasgow and Clyde","Oro-facial clefts",20,"",12173,16.4,""],
    [722,2017,"Greater Glasgow and Clyde","Gastro-intestinal conditions",38,"",12173,31.2,""],
    [723,2017,"Greater Glasgow and Clyde","Abdominal wall defects",8,"",12173,6.6,""],
    [724,2017,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",32,"",12173,26.3,""],
    [725,2017,"Greater Glasgow and Clyde","Genital conditions",49,"",12173,40.3,""],
    [726,2017,"Greater Glasgow and Clyde","Limb conditions",44,"",12173,36.1,""],
    [727,2017,"Greater Glasgow and Clyde","Other conditions/syndromes",13,"",12173,10.7,""],
    [728,2017,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",75,"",12173,61.6,""],
    [729,2017,"Highland","All major congenital conditions registerable by EUROCAT",128,"",2762,463.4,""],
    [732,2017,"Highland","Ear, face and neck conditions",0,"",2762,0,""],
    [733,2017,"Highland","Congenital heart diseases (CHD)",66,"",2762,239,""],
    [735,2017,"Highland","Oro-facial clefts",8,"",2762,29,""],
    [736,2017,"Highland","Gastro-intestinal conditions",5,"",2762,18.1,""],
    [739,2017,"Highland","Genital conditions",9,"",2762,32.6,""],
    [740,2017,"Highland","Limb conditions",13,"",2762,47.1,""],
    [741,2017,"Highland","Other conditions/syndromes",7,"",2762,25.3,""],
    [742,2017,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",12,"",2762,43.4,""],
    [743,2017,"Lanarkshire","All major congenital conditions registerable by EUROCAT",202,"",6798,297.1,""],
    [744,2017,"Lanarkshire","Nervous system conditions",21,"",6798,30.9,""],
    [745,2017,"Lanarkshire","Eye conditions",5,"",6798,7.4,""],
    [746,2017,"Lanarkshire","Ear, face and neck conditions",0,"",6798,0,""],
    [747,2017,"Lanarkshire","Congenital heart diseases (CHD)",66,"",6798,97.1,""],
    [749,2017,"Lanarkshire","Oro-facial clefts",15,"",6798,22.1,""],
    [750,2017,"Lanarkshire","Gastro-intestinal conditions",18,"",6798,26.5,""],
    [752,2017,"Lanarkshire","Kidney and urinary tract conditions",23,"",6798,33.8,""],
    [753,2017,"Lanarkshire","Genital conditions",24,"",6798,35.3,""],
    [754,2017,"Lanarkshire","Limb conditions",26,"",6798,38.2,""],
    [755,2017,"Lanarkshire","Other conditions/syndromes",7,"",6798,10.3,""],
    [756,2017,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",24,"",6798,35.3,""],
    [757,2017,"Lothian","All major congenital conditions registerable by EUROCAT",312,"",9060,344.4,""],
    [758,2017,"Lothian","Nervous system conditions",24,"",9060,26.5,""],
    [759,2017,"Lothian","Eye conditions",7,"",9060,7.7,""],
    [761,2017,"Lothian","Congenital heart diseases (CHD)",50,"",9060,55.2,""],
    [763,2017,"Lothian","Oro-facial clefts",17,"",9060,18.8,""],
    [764,2017,"Lothian","Gastro-intestinal conditions",23,"",9060,25.4,""],
    [765,2017,"Lothian","Abdominal wall defects",5,"",9060,5.5,""],
    [766,2017,"Lothian","Kidney and urinary tract conditions",18,"",9060,19.9,""],
    [767,2017,"Lothian","Genital conditions",58,"",9060,64,""],
    [768,2017,"Lothian","Limb conditions",53,"",9060,58.5,""],
    [769,2017,"Lothian","Other conditions/syndromes",12,"",9060,13.2,""],
    [770,2017,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",59,"",9060,65.1,""],
    [771,2017,"Orkney","All major congenital conditions registerable by EUROCAT",6,"",183,327.9,""],
    [773,2017,"Orkney","Eye conditions",0,"",183,0,""],
    [774,2017,"Orkney","Ear, face and neck conditions",0,"",183,0,""],
    [776,2017,"Orkney","Respiratory conditions",0,"",183,0,""],
    [778,2017,"Orkney","Gastro-intestinal conditions",0,"",183,0,""],
    [779,2017,"Orkney","Abdominal wall defects",0,"",183,0,""],
    [781,2017,"Orkney","Genital conditions",0,"",183,0,""],
    [783,2017,"Orkney","Other conditions/syndromes",0,"",183,0,""],
    [784,2017,"Orkney","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",183,0,""],
    [785,2017,"Shetland","All major congenital conditions registerable by EUROCAT",5,"",220,227.3,""],
    [786,2017,"Shetland","Nervous system conditions",0,"",220,0,""],
    [787,2017,"Shetland","Eye conditions",0,"",220,0,""],
    [788,2017,"Shetland","Ear, face and neck conditions",0,"",220,0,""],
    [790,2017,"Shetland","Respiratory conditions",0,"",220,0,""],
    [791,2017,"Shetland","Oro-facial clefts",0,"",220,0,""],
    [792,2017,"Shetland","Gastro-intestinal conditions",0,"",220,0,""],
    [793,2017,"Shetland","Abdominal wall defects",0,"",220,0,""],
    [794,2017,"Shetland","Kidney and urinary tract conditions",0,"",220,0,""],
    [797,2017,"Shetland","Other conditions/syndromes",0,"",220,0,""],
    [799,2017,"Tayside","All major congenital conditions registerable by EUROCAT",78,"",3791,205.8,""],
    [800,2017,"Tayside","Nervous system conditions",6,"",3791,15.8,""],
    [802,2017,"Tayside","Ear, face and neck conditions",0,"",3791,0,""],
    [803,2017,"Tayside","Congenital heart diseases (CHD)",19,"",3791,50.1,""],
    [805,2017,"Tayside","Oro-facial clefts",6,"",3791,15.8,""],
    [806,2017,"Tayside","Gastro-intestinal conditions",12,"",3791,31.7,""],
    [810,2017,"Tayside","Limb conditions",8,"",3791,21.1,""],
    [812,2017,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",3791,39.6,""],
    [813,2017,"Total","All major congenital conditions registerable by EUROCAT",1745,"",53170,328.2,""],
    [814,2017,"Total","Nervous system conditions",169,"",53170,31.8,""],
    [815,2017,"Total","Eye conditions",40,"",53170,7.5,""],
    [816,2017,"Total","Ear, face and neck conditions",6,"",53170,1.1,""],
    [817,2017,"Total","Congenital heart diseases (CHD)",492,"",53170,92.5,""],
    [818,2017,"Total","Respiratory conditions",26,"",53170,4.9,""],
    [819,2017,"Total","Oro-facial clefts",90,"",53170,16.9,""],
    [820,2017,"Total","Gastro-intestinal conditions",145,"",53170,27.3,""],
    [821,2017,"Total","Abdominal wall defects",32,"",53170,6,""],
    [822,2017,"Total","Kidney and urinary tract conditions",152,"",53170,28.6,""],
    [823,2017,"Total","Genital conditions",212,"",53170,39.9,""],
    [824,2017,"Total","Limb conditions",220,"",53170,41.4,""],
    [825,2017,"Total","Other conditions/syndromes",74,"",53170,13.9,""],
    [826,2017,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",275,"",53170,51.7,""],
    [827,2017,"Western Isles","All major congenital conditions registerable by EUROCAT",6,"",217,276.5,""],
    [828,2017,"Western Isles","Nervous system conditions",0,"",217,0,""],
    [829,2017,"Western Isles","Eye conditions",0,"",217,0,""],
    [830,2017,"Western Isles","Ear, face and neck conditions",0,"",217,0,""],
    [831,2017,"Western Isles","Congenital heart diseases (CHD)",6,"",217,276.5,""],
    [832,2017,"Western Isles","Respiratory conditions",0,"",217,0,""],
    [833,2017,"Western Isles","Oro-facial clefts",0,"",217,0,""],
    [834,2017,"Western Isles","Gastro-intestinal conditions",0,"",217,0,""],
    [835,2017,"Western Isles","Abdominal wall defects",0,"",217,0,""],
    [836,2017,"Western Isles","Kidney and urinary tract conditions",0,"",217,0,""],
    [837,2017,"Western Isles","Genital conditions",0,"",217,0,""],
    [838,2017,"Western Isles","Limb conditions",0,"",217,0,""],
    [839,2017,"Western Isles","Other conditions/syndromes",0,"",217,0,""],
    [840,2017,"Western Isles","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",217,0,""],
    [841,2016,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",148,"",3490,424.1,""],
    [842,2016,"Ayrshire and Arran","Nervous system conditions",20,"",3490,57.3,""],
    [844,2016,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3490,0,""],
    [845,2016,"Ayrshire and Arran","Congenital heart diseases (CHD)",55,"",3490,157.6,""],
    [846,2016,"Ayrshire and Arran","Respiratory conditions",0,"",3490,0,""],
    [848,2016,"Ayrshire and Arran","Gastro-intestinal conditions",9,"",3490,25.8,""],
    [850,2016,"Ayrshire and Arran","Kidney and urinary tract conditions",15,"",3490,43,""],
    [851,2016,"Ayrshire and Arran","Genital conditions",13,"",3490,37.2,""],
    [852,2016,"Ayrshire and Arran","Limb conditions",18,"",3490,51.6,""],
    [853,2016,"Ayrshire and Arran","Other conditions/syndromes",7,"",3490,20.1,""],
    [854,2016,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",17,"",3490,48.7,""],
    [855,2016,"Borders","All major congenital conditions registerable by EUROCAT",22,"",985,223.4,""],
    [857,2016,"Borders","Eye conditions",0,"",985,0,""],
    [858,2016,"Borders","Ear, face and neck conditions",0,"",985,0,""],
    [859,2016,"Borders","Congenital heart diseases (CHD)",6,"",985,60.9,""],
    [860,2016,"Borders","Respiratory conditions",0,"",985,0,""],
    [863,2016,"Borders","Abdominal wall defects",0,"",985,0,""],
    [869,2016,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",33,"",1297,254.4,""],
    [872,2016,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1297,0,""],
    [873,2016,"Dumfries and Galloway","Congenital heart diseases (CHD)",9,"",1297,69.4,""],
    [878,2016,"Dumfries and Galloway","Kidney and urinary tract conditions",5,"",1297,38.6,""],
    [882,2016,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",6,"",1297,46.3,""],
    [883,2016,"Fife","All major congenital conditions registerable by EUROCAT",95,"",3722,255.2,""],
    [884,2016,"Fife","Nervous system conditions",13,"",3722,34.9,""],
    [887,2016,"Fife","Congenital heart diseases (CHD)",24,"",3722,64.5,""],
    [889,2016,"Fife","Oro-facial clefts",9,"",3722,24.2,""],
    [890,2016,"Fife","Gastro-intestinal conditions",9,"",3722,24.2,""],
    [892,2016,"Fife","Kidney and urinary tract conditions",12,"",3722,32.2,""],
    [893,2016,"Fife","Genital conditions",8,"",3722,21.5,""],
    [894,2016,"Fife","Limb conditions",11,"",3722,29.6,""],
    [895,2016,"Fife","Other conditions/syndromes",9,"",3722,24.2,""],
    [896,2016,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",22,"",3722,59.1,""],
    [897,2016,"Forth Valley","All major congenital conditions registerable by EUROCAT",78,"",2915,267.6,""],
    [900,2016,"Forth Valley","Ear, face and neck conditions",0,"",2915,0,""],
    [901,2016,"Forth Valley","Congenital heart diseases (CHD)",19,"",2915,65.2,""],
    [903,2016,"Forth Valley","Oro-facial clefts",5,"",2915,17.2,""],
    [904,2016,"Forth Valley","Gastro-intestinal conditions",8,"",2915,27.4,""],
    [905,2016,"Forth Valley","Abdominal wall defects",0,"",2915,0,""],
    [906,2016,"Forth Valley","Kidney and urinary tract conditions",11,"",2915,37.7,""],
    [907,2016,"Forth Valley","Genital conditions",7,"",2915,24,""],
    [908,2016,"Forth Valley","Limb conditions",5,"",2915,17.2,""],
    [910,2016,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",18,"",2915,61.7,""],
    [911,2016,"Grampian","All major congenital conditions registerable by EUROCAT",276,"",6283,439.3,""],
    [912,2016,"Grampian","Nervous system conditions",31,"",6283,49.3,""],
    [913,2016,"Grampian","Eye conditions",6,"",6283,9.5,""],
    [914,2016,"Grampian","Ear, face and neck conditions",0,"",6283,0,""],
    [915,2016,"Grampian","Congenital heart diseases (CHD)",83,"",6283,132.1,""],
    [916,2016,"Grampian","Respiratory conditions",0,"",6283,0,""],
    [917,2016,"Grampian","Oro-facial clefts",15,"",6283,23.9,""],
    [918,2016,"Grampian","Gastro-intestinal conditions",17,"",6283,27.1,""],
    [920,2016,"Grampian","Kidney and urinary tract conditions",16,"",6283,25.5,""],
    [921,2016,"Grampian","Genital conditions",42,"",6283,66.8,""],
    [922,2016,"Grampian","Limb conditions",41,"",6283,65.3,""],
    [923,2016,"Grampian","Other conditions/syndromes",11,"",6283,17.5,""],
    [924,2016,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",34,"",6283,54.1,""],
    [925,2016,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",480,"",12180,394.1,""],
    [926,2016,"Greater Glasgow and Clyde","Nervous system conditions",34,"",12180,27.9,""],
    [927,2016,"Greater Glasgow and Clyde","Eye conditions",19,"",12180,15.6,""],
    [929,2016,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",162,"",12180,133,""],
    [931,2016,"Greater Glasgow and Clyde","Oro-facial clefts",19,"",12180,15.6,""],
    [932,2016,"Greater Glasgow and Clyde","Gastro-intestinal conditions",37,"",12180,30.4,""],
    [933,2016,"Greater Glasgow and Clyde","Abdominal wall defects",13,"",12180,10.7,""],
    [934,2016,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",47,"",12180,38.6,""],
    [935,2016,"Greater Glasgow and Clyde","Genital conditions",40,"",12180,32.8,""],
    [936,2016,"Greater Glasgow and Clyde","Limb conditions",40,"",12180,32.8,""],
    [937,2016,"Greater Glasgow and Clyde","Other conditions/syndromes",23,"",12180,18.9,""],
    [938,2016,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",67,"",12180,55,""],
    [939,2016,"Highland","All major congenital conditions registerable by EUROCAT",120,"",2841,422.4,""],
    [940,2016,"Highland","Nervous system conditions",11,"",2841,38.7,""],
    [942,2016,"Highland","Ear, face and neck conditions",0,"",2841,0,""],
    [943,2016,"Highland","Congenital heart diseases (CHD)",44,"",2841,154.9,""],
    [945,2016,"Highland","Oro-facial clefts",5,"",2841,17.6,""],
    [946,2016,"Highland","Gastro-intestinal conditions",20,"",2841,70.4,""],
    [947,2016,"Highland","Abdominal wall defects",5,"",2841,17.6,""],
    [948,2016,"Highland","Kidney and urinary tract conditions",7,"",2841,24.6,""],
    [949,2016,"Highland","Genital conditions",19,"",2841,66.9,""],
    [950,2016,"Highland","Limb conditions",12,"",2841,42.2,""],
    [951,2016,"Highland","Other conditions/syndromes",7,"",2841,24.6,""],
    [952,2016,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",2841,52.8,""],
    [953,2016,"Lanarkshire","All major congenital conditions registerable by EUROCAT",193,"",6860,281.3,""],
    [954,2016,"Lanarkshire","Nervous system conditions",15,"",6860,21.9,""],
    [956,2016,"Lanarkshire","Ear, face and neck conditions",0,"",6860,0,""],
    [957,2016,"Lanarkshire","Congenital heart diseases (CHD)",64,"",6860,93.3,""],
    [959,2016,"Lanarkshire","Oro-facial clefts",8,"",6860,11.7,""],
    [960,2016,"Lanarkshire","Gastro-intestinal conditions",9,"",6860,13.1,""],
    [961,2016,"Lanarkshire","Abdominal wall defects",5,"",6860,7.3,""],
    [962,2016,"Lanarkshire","Kidney and urinary tract conditions",18,"",6860,26.2,""],
    [963,2016,"Lanarkshire","Genital conditions",19,"",6860,27.7,""],
    [964,2016,"Lanarkshire","Limb conditions",25,"",6860,36.4,""],
    [965,2016,"Lanarkshire","Other conditions/syndromes",8,"",6860,11.7,""],
    [966,2016,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",27,"",6860,39.4,""],
    [967,2016,"Lothian","All major congenital conditions registerable by EUROCAT",406,"",9459,429.2,""],
    [968,2016,"Lothian","Nervous system conditions",36,"",9459,38.1,""],
    [971,2016,"Lothian","Congenital heart diseases (CHD)",58,"",9459,61.3,""],
    [973,2016,"Lothian","Oro-facial clefts",19,"",9459,20.1,""],
    [974,2016,"Lothian","Gastro-intestinal conditions",23,"",9459,24.3,""],
    [975,2016,"Lothian","Abdominal wall defects",6,"",9459,6.3,""],
    [976,2016,"Lothian","Kidney and urinary tract conditions",38,"",9459,40.2,""],
    [977,2016,"Lothian","Genital conditions",58,"",9459,61.3,""],
    [978,2016,"Lothian","Limb conditions",106,"",9459,112.1,""],
    [979,2016,"Lothian","Other conditions/syndromes",11,"",9459,11.6,""],
    [980,2016,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",69,"",9459,72.9,""],
    [982,2016,"Orkney","Nervous system conditions",0,"",184,0,""],
    [984,2016,"Orkney","Ear, face and neck conditions",0,"",184,0,""],
    [986,2016,"Orkney","Respiratory conditions",0,"",184,0,""],
    [987,2016,"Orkney","Oro-facial clefts",0,"",184,0,""],
    [988,2016,"Orkney","Gastro-intestinal conditions",0,"",184,0,""],
    [989,2016,"Orkney","Abdominal wall defects",0,"",184,0,""],
    [991,2016,"Orkney","Genital conditions",0,"",184,0,""],
    [992,2016,"Orkney","Limb conditions",0,"",184,0,""],
    [993,2016,"Orkney","Other conditions/syndromes",0,"",184,0,""],
    [994,2016,"Orkney","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",184,0,""],
    [995,2016,"Shetland","All major congenital conditions registerable by EUROCAT",8,"",262,305.3,""],
    [996,2016,"Shetland","Nervous system conditions",0,"",262,0,""],
    [997,2016,"Shetland","Eye conditions",0,"",262,0,""],
    [1000,2016,"Shetland","Respiratory conditions",0,"",262,0,""],
    [1001,2016,"Shetland","Oro-facial clefts",0,"",262,0,""],
    [1003,2016,"Shetland","Abdominal wall defects",0,"",262,0,""],
    [1004,2016,"Shetland","Kidney and urinary tract conditions",0,"",262,0,""],
    [1006,2016,"Shetland","Limb conditions",0,"",262,0,""],
    [1008,2016,"Shetland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",262,0,""],
    [1009,2016,"Tayside","All major congenital conditions registerable by EUROCAT",123,"",3971,309.7,""],
    [1010,2016,"Tayside","Nervous system conditions",12,"",3971,30.2,""],
    [1011,2016,"Tayside","Eye conditions",7,"",3971,17.6,""],
    [1012,2016,"Tayside","Ear, face and neck conditions",0,"",3971,0,""],
    [1013,2016,"Tayside","Congenital heart diseases (CHD)",25,"",3971,63,""],
    [1015,2016,"Tayside","Oro-facial clefts",12,"",3971,30.2,""],
    [1016,2016,"Tayside","Gastro-intestinal conditions",12,"",3971,30.2,""],
    [1017,2016,"Tayside","Abdominal wall defects",6,"",3971,15.1,""],
    [1018,2016,"Tayside","Kidney and urinary tract conditions",8,"",3971,20.1,""],
    [1019,2016,"Tayside","Genital conditions",22,"",3971,55.4,""],
    [1020,2016,"Tayside","Limb conditions",10,"",3971,25.2,""],
    [1022,2016,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",29,"",3971,73,""],
    [1023,2016,"Total","All major congenital conditions registerable by EUROCAT",1987,"",54818,362.5,""],
    [1024,2016,"Total","Nervous system conditions",184,"",54818,33.6,""],
    [1025,2016,"Total","Eye conditions",48,"",54818,8.8,""],
    [1026,2016,"Total","Ear, face and neck conditions",9,"",54818,1.6,""],
    [1027,2016,"Total","Congenital heart diseases (CHD)",554,"",54818,101.1,""],
    [1028,2016,"Total","Respiratory conditions",21,"",54818,3.8,""],
    [1029,2016,"Total","Oro-facial clefts",98,"",54818,17.9,""],
    [1030,2016,"Total","Gastro-intestinal conditions",150,"",54818,27.4,""],
    [1031,2016,"Total","Abdominal wall defects",43,"",54818,7.8,""],
    [1032,2016,"Total","Kidney and urinary tract conditions",182,"",54818,33.2,""],
    [1033,2016,"Total","Genital conditions",233,"",54818,42.5,""],
    [1034,2016,"Total","Limb conditions",271,"",54818,49.4,""],
    [1035,2016,"Total","Other conditions/syndromes",86,"",54818,15.7,""],
    [1036,2016,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",306,"",54818,55.8,""],
    [1038,2016,"Western Isles","Nervous system conditions",0,"",241,0,""],
    [1039,2016,"Western Isles","Eye conditions",0,"",241,0,""],
    [1040,2016,"Western Isles","Ear, face and neck conditions",0,"",241,0,""],
    [1041,2016,"Western Isles","Congenital heart diseases (CHD)",0,"",241,0,""],
    [1042,2016,"Western Isles","Respiratory conditions",0,"",241,0,""],
    [1043,2016,"Western Isles","Oro-facial clefts",0,"",241,0,""],
    [1044,2016,"Western Isles","Gastro-intestinal conditions",0,"",241,0,""],
    [1045,2016,"Western Isles","Abdominal wall defects",0,"",241,0,""],
    [1046,2016,"Western Isles","Kidney and urinary tract conditions",0,"",241,0,""],
    [1047,2016,"Western Isles","Genital conditions",0,"",241,0,""],
    [1048,2016,"Western Isles","Limb conditions",0,"",241,0,""],
    [1050,2016,"Western Isles","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",241,0,""],
    [1051,2015,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",135,"",3585,376.6,""],
    [1052,2015,"Ayrshire and Arran","Nervous system conditions",9,"",3585,25.1,""],
    [1055,2015,"Ayrshire and Arran","Congenital heart diseases (CHD)",36,"",3585,100.4,""],
    [1057,2015,"Ayrshire and Arran","Oro-facial clefts",0,"",3585,0,""],
    [1058,2015,"Ayrshire and Arran","Gastro-intestinal conditions",8,"",3585,22.3,""],
    [1060,2015,"Ayrshire and Arran","Kidney and urinary tract conditions",15,"",3585,41.8,""],
    [1061,2015,"Ayrshire and Arran","Genital conditions",28,"",3585,78.1,""],
    [1062,2015,"Ayrshire and Arran","Limb conditions",17,"",3585,47.4,""],
    [1063,2015,"Ayrshire and Arran","Other conditions/syndromes",9,"",3585,25.1,""],
    [1064,2015,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",17,"",3585,47.4,""],
    [1065,2015,"Borders","All major congenital conditions registerable by EUROCAT",15,"",954,157.2,""],
    [1073,2015,"Borders","Abdominal wall defects",0,"",954,0,""],
    [1079,2015,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",35,"",1277,274.1,""],
    [1081,2015,"Dumfries and Galloway","Eye conditions",0,"",1277,0,""],
    [1083,2015,"Dumfries and Galloway","Congenital heart diseases (CHD)",8,"",1277,62.6,""],
    [1085,2015,"Dumfries and Galloway","Oro-facial clefts",5,"",1277,39.2,""],
    [1088,2015,"Dumfries and Galloway","Kidney and urinary tract conditions",5,"",1277,39.2,""],
    [1092,2015,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",9,"",1277,70.5,""],
    [1093,2015,"Fife","All major congenital conditions registerable by EUROCAT",87,"",3769,230.8,""],
    [1094,2015,"Fife","Nervous system conditions",11,"",3769,29.2,""],
    [1095,2015,"Fife","Eye conditions",0,"",3769,0,""],
    [1097,2015,"Fife","Congenital heart diseases (CHD)",29,"",3769,76.9,""],
    [1099,2015,"Fife","Oro-facial clefts",8,"",3769,21.2,""],
    [1102,2015,"Fife","Kidney and urinary tract conditions",13,"",3769,34.5,""],
    [1104,2015,"Fife","Limb conditions",14,"",3769,37.1,""],
    [1105,2015,"Fife","Other conditions/syndromes",5,"",3769,13.3,""],
    [1106,2015,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",3769,42.5,""],
    [1107,2015,"Forth Valley","All major congenital conditions registerable by EUROCAT",111,"",2951,376.1,""],
    [1108,2015,"Forth Valley","Nervous system conditions",15,"",2951,50.8,""],
    [1109,2015,"Forth Valley","Eye conditions",0,"",2951,0,""],
    [1111,2015,"Forth Valley","Congenital heart diseases (CHD)",33,"",2951,111.8,""],
    [1112,2015,"Forth Valley","Respiratory conditions",0,"",2951,0,""],
    [1116,2015,"Forth Valley","Kidney and urinary tract conditions",13,"",2951,44.1,""],
    [1117,2015,"Forth Valley","Genital conditions",17,"",2951,57.6,""],
    [1118,2015,"Forth Valley","Limb conditions",13,"",2951,44.1,""],
    [1119,2015,"Forth Valley","Other conditions/syndromes",8,"",2951,27.1,""],
    [1120,2015,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",21,"",2951,71.2,""],
    [1121,2015,"Grampian","All major congenital conditions registerable by EUROCAT",223,"",6422,347.2,""],
    [1122,2015,"Grampian","Nervous system conditions",14,"",6422,21.8,""],
    [1125,2015,"Grampian","Congenital heart diseases (CHD)",69,"",6422,107.4,""],
    [1127,2015,"Grampian","Oro-facial clefts",10,"",6422,15.6,""],
    [1128,2015,"Grampian","Gastro-intestinal conditions",11,"",6422,17.1,""],
    [1129,2015,"Grampian","Abdominal wall defects",5,"",6422,7.8,""],
    [1130,2015,"Grampian","Kidney and urinary tract conditions",15,"",6422,23.4,""],
    [1131,2015,"Grampian","Genital conditions",25,"",6422,38.9,""],
    [1132,2015,"Grampian","Limb conditions",39,"",6422,60.7,""],
    [1133,2015,"Grampian","Other conditions/syndromes",11,"",6422,17.1,""],
    [1134,2015,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",40,"",6422,62.3,""],
    [1135,2015,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",486,"",12245,396.9,""],
    [1136,2015,"Greater Glasgow and Clyde","Nervous system conditions",43,"",12245,35.1,""],
    [1137,2015,"Greater Glasgow and Clyde","Eye conditions",23,"",12245,18.8,""],
    [1139,2015,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",155,"",12245,126.6,""],
    [1140,2015,"Greater Glasgow and Clyde","Respiratory conditions",5,"",12245,4.1,""],
    [1141,2015,"Greater Glasgow and Clyde","Oro-facial clefts",32,"",12245,26.1,""],
    [1142,2015,"Greater Glasgow and Clyde","Gastro-intestinal conditions",31,"",12245,25.3,""],
    [1143,2015,"Greater Glasgow and Clyde","Abdominal wall defects",9,"",12245,7.3,""],
    [1144,2015,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",65,"",12245,53.1,""],
    [1145,2015,"Greater Glasgow and Clyde","Genital conditions",36,"",12245,29.4,""],
    [1146,2015,"Greater Glasgow and Clyde","Limb conditions",49,"",12245,40,""],
    [1147,2015,"Greater Glasgow and Clyde","Other conditions/syndromes",18,"",12245,14.7,""],
    [1148,2015,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",70,"",12245,57.2,""],
    [1149,2015,"Highland","All major congenital conditions registerable by EUROCAT",142,"",2921,486.1,""],
    [1150,2015,"Highland","Nervous system conditions",11,"",2921,37.7,""],
    [1153,2015,"Highland","Congenital heart diseases (CHD)",52,"",2921,178,""],
    [1156,2015,"Highland","Gastro-intestinal conditions",11,"",2921,37.7,""],
    [1157,2015,"Highland","Abdominal wall defects",7,"",2921,24,""],
    [1158,2015,"Highland","Kidney and urinary tract conditions",12,"",2921,41.1,""],
    [1159,2015,"Highland","Genital conditions",15,"",2921,51.4,""],
    [1160,2015,"Highland","Limb conditions",18,"",2921,61.6,""],
    [1161,2015,"Highland","Other conditions/syndromes",5,"",2921,17.1,""],
    [1162,2015,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",22,"",2921,75.3,""],
    [1163,2015,"Lanarkshire","All major congenital conditions registerable by EUROCAT",279,"",6963,400.7,""],
    [1164,2015,"Lanarkshire","Nervous system conditions",20,"",6963,28.7,""],
    [1167,2015,"Lanarkshire","Congenital heart diseases (CHD)",93,"",6963,133.6,""],
    [1169,2015,"Lanarkshire","Oro-facial clefts",8,"",6963,11.5,""],
    [1170,2015,"Lanarkshire","Gastro-intestinal conditions",29,"",6963,41.6,""],
    [1171,2015,"Lanarkshire","Abdominal wall defects",5,"",6963,7.2,""],
    [1172,2015,"Lanarkshire","Kidney and urinary tract conditions",30,"",6963,43.1,""],
    [1173,2015,"Lanarkshire","Genital conditions",20,"",6963,28.7,""],
    [1174,2015,"Lanarkshire","Limb conditions",32,"",6963,46,""],
    [1175,2015,"Lanarkshire","Other conditions/syndromes",11,"",6963,15.8,""],
    [1176,2015,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",38,"",6963,54.6,""],
    [1177,2015,"Lothian","All major congenital conditions registerable by EUROCAT",410,"",9354,438.3,""],
    [1178,2015,"Lothian","Nervous system conditions",28,"",9354,29.9,""],
    [1181,2015,"Lothian","Congenital heart diseases (CHD)",59,"",9354,63.1,""],
    [1183,2015,"Lothian","Oro-facial clefts",12,"",9354,12.8,""],
    [1184,2015,"Lothian","Gastro-intestinal conditions",12,"",9354,12.8,""],
    [1185,2015,"Lothian","Abdominal wall defects",6,"",9354,6.4,""],
    [1186,2015,"Lothian","Kidney and urinary tract conditions",19,"",9354,20.3,""],
    [1187,2015,"Lothian","Genital conditions",61,"",9354,65.2,""],
    [1188,2015,"Lothian","Limb conditions",137,"",9354,146.5,""],
    [1189,2015,"Lothian","Other conditions/syndromes",12,"",9354,12.8,""],
    [1190,2015,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",61,"",9354,65.2,""],
    [1191,2015,"Orkney","All major congenital conditions registerable by EUROCAT",7,"",191,366.5,""],
    [1192,2015,"Orkney","Nervous system conditions",0,"",191,0,""],
    [1193,2015,"Orkney","Eye conditions",0,"",191,0,""],
    [1196,2015,"Orkney","Respiratory conditions",0,"",191,0,""],
    [1197,2015,"Orkney","Oro-facial clefts",0,"",191,0,""],
    [1199,2015,"Orkney","Abdominal wall defects",0,"",191,0,""],
    [1201,2015,"Orkney","Genital conditions",0,"",191,0,""],
    [1202,2015,"Orkney","Limb conditions",0,"",191,0,""],
    [1203,2015,"Orkney","Other conditions/syndromes",0,"",191,0,""],
    [1205,2015,"Shetland","All major congenital conditions registerable by EUROCAT",6,"",232,258.6,""],
    [1206,2015,"Shetland","Nervous system conditions",0,"",232,0,""],
    [1207,2015,"Shetland","Eye conditions",0,"",232,0,""],
    [1210,2015,"Shetland","Respiratory conditions",0,"",232,0,""],
    [1211,2015,"Shetland","Oro-facial clefts",0,"",232,0,""],
    [1213,2015,"Shetland","Abdominal wall defects",0,"",232,0,""],
    [1214,2015,"Shetland","Kidney and urinary tract conditions",0,"",232,0,""],
    [1215,2015,"Shetland","Genital conditions",0,"",232,0,""],
    [1217,2015,"Shetland","Other conditions/syndromes",0,"",232,0,""],
    [1219,2015,"Tayside","All major congenital conditions registerable by EUROCAT",123,"",3986,308.6,""],
    [1220,2015,"Tayside","Nervous system conditions",15,"",3986,37.6,""],
    [1223,2015,"Tayside","Congenital heart diseases (CHD)",27,"",3986,67.7,""],
    [1225,2015,"Tayside","Oro-facial clefts",9,"",3986,22.6,""],
    [1226,2015,"Tayside","Gastro-intestinal conditions",14,"",3986,35.1,""],
    [1228,2015,"Tayside","Kidney and urinary tract conditions",11,"",3986,27.6,""],
    [1229,2015,"Tayside","Genital conditions",21,"",3986,52.7,""],
    [1230,2015,"Tayside","Limb conditions",11,"",3986,27.6,""],
    [1231,2015,"Tayside","Other conditions/syndromes",9,"",3986,22.6,""],
    [1232,2015,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",3986,37.6,""],
    [1233,2015,"Total","All major congenital conditions registerable by EUROCAT",2066,"",55317,373.5,""],
    [1234,2015,"Total","Nervous system conditions",170,"",55317,30.7,""],
    [1235,2015,"Total","Eye conditions",43,"",55317,7.8,""],
    [1236,2015,"Total","Ear, face and neck conditions",3,"",55317,0.5,""],
    [1237,2015,"Total","Congenital heart diseases (CHD)",571,"",55317,103.2,""],
    [1238,2015,"Total","Respiratory conditions",19,"",55317,3.4,""],
    [1239,2015,"Total","Oro-facial clefts",94,"",55317,17,""],
    [1240,2015,"Total","Gastro-intestinal conditions",135,"",55317,24.4,""],
    [1241,2015,"Total","Abdominal wall defects",46,"",55317,8.3,""],
    [1242,2015,"Total","Kidney and urinary tract conditions",202,"",55317,36.5,""],
    [1243,2015,"Total","Genital conditions",234,"",55317,42.3,""],
    [1244,2015,"Total","Limb conditions",340,"",55317,61.5,""],
    [1245,2015,"Total","Other conditions/syndromes",92,"",55317,16.6,""],
    [1246,2015,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",315,"",55317,56.9,""],
    [1247,2015,"Western Isles","All major congenital conditions registerable by EUROCAT",7,"",226,309.7,""],
    [1249,2015,"Western Isles","Eye conditions",0,"",226,0,""],
    [1252,2015,"Western Isles","Respiratory conditions",0,"",226,0,""],
    [1253,2015,"Western Isles","Oro-facial clefts",0,"",226,0,""],
    [1255,2015,"Western Isles","Abdominal wall defects",0,"",226,0,""],
    [1256,2015,"Western Isles","Kidney and urinary tract conditions",0,"",226,0,""],
    [1259,2015,"Western Isles","Other conditions/syndromes",0,"",226,0,""],
    [1260,2015,"Western Isles","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",226,0,""],
    [1261,2014,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",122,"",3601,338.8,""],
    [1262,2014,"Ayrshire and Arran","Nervous system conditions",13,"",3601,36.1,""],
    [1265,2014,"Ayrshire and Arran","Congenital heart diseases (CHD)",24,"",3601,66.6,""],
    [1266,2014,"Ayrshire and Arran","Respiratory conditions",0,"",3601,0,""],
    [1267,2014,"Ayrshire and Arran","Oro-facial clefts",8,"",3601,22.2,""],
    [1270,2014,"Ayrshire and Arran","Kidney and urinary tract conditions",17,"",3601,47.2,""],
    [1271,2014,"Ayrshire and Arran","Genital conditions",17,"",3601,47.2,""],
    [1272,2014,"Ayrshire and Arran","Limb conditions",21,"",3601,58.3,""],
    [1273,2014,"Ayrshire and Arran","Other conditions/syndromes",6,"",3601,16.7,""],
    [1274,2014,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",17,"",3601,47.2,""],
    [1275,2014,"Borders","All major congenital conditions registerable by EUROCAT",9,"",995,90.5,""],
    [1277,2014,"Borders","Eye conditions",0,"",995,0,""],
    [1278,2014,"Borders","Ear, face and neck conditions",0,"",995,0,""],
    [1279,2014,"Borders","Congenital heart diseases (CHD)",5,"",995,50.3,""],
    [1280,2014,"Borders","Respiratory conditions",0,"",995,0,""],
    [1281,2014,"Borders","Oro-facial clefts",0,"",995,0,""],
    [1283,2014,"Borders","Abdominal wall defects",0,"",995,0,""],
    [1284,2014,"Borders","Kidney and urinary tract conditions",0,"",995,0,""],
    [1285,2014,"Borders","Genital conditions",0,"",995,0,""],
    [1287,2014,"Borders","Other conditions/syndromes",0,"",995,0,""],
    [1289,2014,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",42,"",1274,329.7,""],
    [1291,2014,"Dumfries and Galloway","Eye conditions",0,"",1274,0,""],
    [1292,2014,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1274,0,""],
    [1293,2014,"Dumfries and Galloway","Congenital heart diseases (CHD)",5,"",1274,39.2,""],
    [1298,2014,"Dumfries and Galloway","Kidney and urinary tract conditions",10,"",1274,78.5,""],
    [1302,2014,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",10,"",1274,78.5,""],
    [1303,2014,"Fife","All major congenital conditions registerable by EUROCAT",93,"",3901,238.4,""],
    [1304,2014,"Fife","Nervous system conditions",11,"",3901,28.2,""],
    [1306,2014,"Fife","Ear, face and neck conditions",0,"",3901,0,""],
    [1307,2014,"Fife","Congenital heart diseases (CHD)",24,"",3901,61.5,""],
    [1308,2014,"Fife","Respiratory conditions",6,"",3901,15.4,""],
    [1310,2014,"Fife","Gastro-intestinal conditions",9,"",3901,23.1,""],
    [1313,2014,"Fife","Genital conditions",6,"",3901,15.4,""],
    [1314,2014,"Fife","Limb conditions",8,"",3901,20.5,""],
    [1315,2014,"Fife","Other conditions/syndromes",6,"",3901,15.4,""],
    [1316,2014,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",20,"",3901,51.3,""],
    [1317,2014,"Forth Valley","All major congenital conditions registerable by EUROCAT",89,"",3095,287.6,""],
    [1318,2014,"Forth Valley","Nervous system conditions",10,"",3095,32.3,""],
    [1320,2014,"Forth Valley","Ear, face and neck conditions",0,"",3095,0,""],
    [1321,2014,"Forth Valley","Congenital heart diseases (CHD)",30,"",3095,96.9,""],
    [1323,2014,"Forth Valley","Oro-facial clefts",7,"",3095,22.6,""],
    [1324,2014,"Forth Valley","Gastro-intestinal conditions",6,"",3095,19.4,""],
    [1326,2014,"Forth Valley","Kidney and urinary tract conditions",11,"",3095,35.5,""],
    [1327,2014,"Forth Valley","Genital conditions",9,"",3095,29.1,""],
    [1328,2014,"Forth Valley","Limb conditions",18,"",3095,58.2,""],
    [1330,2014,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",7,"",3095,22.6,""],
    [1331,2014,"Grampian","All major congenital conditions registerable by EUROCAT",240,"",6341,378.5,""],
    [1332,2014,"Grampian","Nervous system conditions",27,"",6341,42.6,""],
    [1333,2014,"Grampian","Eye conditions",7,"",6341,11,""],
    [1335,2014,"Grampian","Congenital heart diseases (CHD)",55,"",6341,86.7,""],
    [1337,2014,"Grampian","Oro-facial clefts",7,"",6341,11,""],
    [1338,2014,"Grampian","Gastro-intestinal conditions",23,"",6341,36.3,""],
    [1339,2014,"Grampian","Abdominal wall defects",8,"",6341,12.6,""],
    [1340,2014,"Grampian","Kidney and urinary tract conditions",17,"",6341,26.8,""],
    [1341,2014,"Grampian","Genital conditions",31,"",6341,48.9,""],
    [1342,2014,"Grampian","Limb conditions",46,"",6341,72.5,""],
    [1343,2014,"Grampian","Other conditions/syndromes",10,"",6341,15.8,""],
    [1344,2014,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",37,"",6341,58.4,""],
    [1345,2014,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",469,"",12761,367.5,""],
    [1346,2014,"Greater Glasgow and Clyde","Nervous system conditions",28,"",12761,21.9,""],
    [1347,2014,"Greater Glasgow and Clyde","Eye conditions",15,"",12761,11.8,""],
    [1349,2014,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",131,"",12761,102.7,""],
    [1350,2014,"Greater Glasgow and Clyde","Respiratory conditions",11,"",12761,8.6,""],
    [1351,2014,"Greater Glasgow and Clyde","Oro-facial clefts",21,"",12761,16.5,""],
    [1352,2014,"Greater Glasgow and Clyde","Gastro-intestinal conditions",35,"",12761,27.4,""],
    [1353,2014,"Greater Glasgow and Clyde","Abdominal wall defects",9,"",12761,7.1,""],
    [1354,2014,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",47,"",12761,36.8,""],
    [1355,2014,"Greater Glasgow and Clyde","Genital conditions",39,"",12761,30.6,""],
    [1356,2014,"Greater Glasgow and Clyde","Limb conditions",62,"",12761,48.6,""],
    [1357,2014,"Greater Glasgow and Clyde","Other conditions/syndromes",14,"",12761,11,""],
    [1358,2014,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",50,"",12761,39.2,""],
    [1359,2014,"Highland","All major congenital conditions registerable by EUROCAT",145,"",3016,480.8,""],
    [1360,2014,"Highland","Nervous system conditions",11,"",3016,36.5,""],
    [1362,2014,"Highland","Ear, face and neck conditions",0,"",3016,0,""],
    [1363,2014,"Highland","Congenital heart diseases (CHD)",80,"",3016,265.3,""],
    [1366,2014,"Highland","Gastro-intestinal conditions",7,"",3016,23.2,""],
    [1369,2014,"Highland","Genital conditions",16,"",3016,53.1,""],
    [1370,2014,"Highland","Limb conditions",12,"",3016,39.8,""],
    [1372,2014,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",19,"",3016,63,""],
    [1373,2014,"Lanarkshire","All major congenital conditions registerable by EUROCAT",218,"",7120,306.2,""],
    [1374,2014,"Lanarkshire","Nervous system conditions",18,"",7120,25.3,""],
    [1375,2014,"Lanarkshire","Eye conditions",7,"",7120,9.8,""],
    [1376,2014,"Lanarkshire","Ear, face and neck conditions",0,"",7120,0,""],
    [1377,2014,"Lanarkshire","Congenital heart diseases (CHD)",61,"",7120,85.7,""],
    [1379,2014,"Lanarkshire","Oro-facial clefts",8,"",7120,11.2,""],
    [1380,2014,"Lanarkshire","Gastro-intestinal conditions",16,"",7120,22.5,""],
    [1382,2014,"Lanarkshire","Kidney and urinary tract conditions",24,"",7120,33.7,""],
    [1383,2014,"Lanarkshire","Genital conditions",23,"",7120,32.3,""],
    [1384,2014,"Lanarkshire","Limb conditions",22,"",7120,30.9,""],
    [1385,2014,"Lanarkshire","Other conditions/syndromes",13,"",7120,18.3,""],
    [1386,2014,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",29,"",7120,40.7,""],
    [1387,2014,"Lothian","All major congenital conditions registerable by EUROCAT",394,"",9644,408.5,""],
    [1388,2014,"Lothian","Nervous system conditions",45,"",9644,46.7,""],
    [1391,2014,"Lothian","Congenital heart diseases (CHD)",57,"",9644,59.1,""],
    [1393,2014,"Lothian","Oro-facial clefts",12,"",9644,12.4,""],
    [1394,2014,"Lothian","Gastro-intestinal conditions",26,"",9644,27,""],
    [1395,2014,"Lothian","Abdominal wall defects",8,"",9644,8.3,""],
    [1396,2014,"Lothian","Kidney and urinary tract conditions",30,"",9644,31.1,""],
    [1397,2014,"Lothian","Genital conditions",62,"",9644,64.3,""],
    [1398,2014,"Lothian","Limb conditions",96,"",9644,99.5,""],
    [1399,2014,"Lothian","Other conditions/syndromes",12,"",9644,12.4,""],
    [1400,2014,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",66,"",9644,68.4,""],
    [1402,2014,"Orkney","Nervous system conditions",0,"",180,0,""],
    [1403,2014,"Orkney","Eye conditions",0,"",180,0,""],
    [1404,2014,"Orkney","Ear, face and neck conditions",0,"",180,0,""],
    [1406,2014,"Orkney","Respiratory conditions",0,"",180,0,""],
    [1408,2014,"Orkney","Gastro-intestinal conditions",0,"",180,0,""],
    [1409,2014,"Orkney","Abdominal wall defects",0,"",180,0,""],
    [1410,2014,"Orkney","Kidney and urinary tract conditions",0,"",180,0,""],
    [1411,2014,"Orkney","Genital conditions",0,"",180,0,""],
    [1413,2014,"Orkney","Other conditions/syndromes",0,"",180,0,""],
    [1415,2014,"Shetland","All major congenital conditions registerable by EUROCAT",5,"",265,188.7,""],
    [1416,2014,"Shetland","Nervous system conditions",0,"",265,0,""],
    [1417,2014,"Shetland","Eye conditions",0,"",265,0,""],
    [1418,2014,"Shetland","Ear, face and neck conditions",0,"",265,0,""],
    [1420,2014,"Shetland","Respiratory conditions",0,"",265,0,""],
    [1421,2014,"Shetland","Oro-facial clefts",0,"",265,0,""],
    [1422,2014,"Shetland","Gastro-intestinal conditions",0,"",265,0,""],
    [1423,2014,"Shetland","Abdominal wall defects",0,"",265,0,""],
    [1424,2014,"Shetland","Kidney and urinary tract conditions",0,"",265,0,""],
    [1427,2014,"Shetland","Other conditions/syndromes",0,"",265,0,""],
    [1428,2014,"Shetland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",265,0,""],
    [1429,2014,"Tayside","All major congenital conditions registerable by EUROCAT",144,"",4195,343.3,""],
    [1430,2014,"Tayside","Nervous system conditions",23,"",4195,54.8,""],
    [1433,2014,"Tayside","Congenital heart diseases (CHD)",33,"",4195,78.7,""],
    [1435,2014,"Tayside","Oro-facial clefts",11,"",4195,26.2,""],
    [1436,2014,"Tayside","Gastro-intestinal conditions",11,"",4195,26.2,""],
    [1439,2014,"Tayside","Genital conditions",23,"",4195,54.8,""],
    [1440,2014,"Tayside","Limb conditions",17,"",4195,40.5,""],
    [1441,2014,"Tayside","Other conditions/syndromes",10,"",4195,23.8,""],
    [1442,2014,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",31,"",4195,73.9,""],
    [1443,2014,"Total","All major congenital conditions registerable by EUROCAT",1983,"",56854,348.8,""],
    [1444,2014,"Total","Nervous system conditions",191,"",56854,33.6,""],
    [1445,2014,"Total","Eye conditions",43,"",56854,7.6,""],
    [1446,2014,"Total","Ear, face and neck conditions",8,"",56854,1.4,""],
    [1447,2014,"Total","Congenital heart diseases (CHD)",511,"",56854,89.9,""],
    [1448,2014,"Total","Respiratory conditions",32,"",56854,5.6,""],
    [1449,2014,"Total","Oro-facial clefts",88,"",56854,15.5,""],
    [1450,2014,"Total","Gastro-intestinal conditions",143,"",56854,25.2,""],
    [1451,2014,"Total","Abdominal wall defects",43,"",56854,7.6,""],
    [1452,2014,"Total","Kidney and urinary tract conditions",181,"",56854,31.8,""],
    [1453,2014,"Total","Genital conditions",231,"",56854,40.6,""],
    [1454,2014,"Total","Limb conditions",310,"",56854,54.5,""],
    [1455,2014,"Total","Other conditions/syndromes",79,"",56854,13.9,""],
    [1456,2014,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",290,"",56854,51,""],
    [1457,2014,"Western Isles","All major congenital conditions registerable by EUROCAT",9,"",214,420.6,""],
    [1458,2014,"Western Isles","Nervous system conditions",0,"",214,0,""],
    [1460,2014,"Western Isles","Ear, face and neck conditions",0,"",214,0,""],
    [1462,2014,"Western Isles","Respiratory conditions",0,"",214,0,""],
    [1467,2014,"Western Isles","Genital conditions",0,"",214,0,""],
    [1468,2014,"Western Isles","Limb conditions",0,"",214,0,""],
    [1471,2013,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",140,"",3650,383.6,""],
    [1472,2013,"Ayrshire and Arran","Nervous system conditions",8,"",3650,21.9,""],
    [1475,2013,"Ayrshire and Arran","Congenital heart diseases (CHD)",39,"",3650,106.8,""],
    [1477,2013,"Ayrshire and Arran","Oro-facial clefts",10,"",3650,27.4,""],
    [1478,2013,"Ayrshire and Arran","Gastro-intestinal conditions",13,"",3650,35.6,""],
    [1480,2013,"Ayrshire and Arran","Kidney and urinary tract conditions",13,"",3650,35.6,""],
    [1481,2013,"Ayrshire and Arran","Genital conditions",16,"",3650,43.8,""],
    [1482,2013,"Ayrshire and Arran","Limb conditions",26,"",3650,71.2,""],
    [1483,2013,"Ayrshire and Arran","Other conditions/syndromes",5,"",3650,13.7,""],
    [1484,2013,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",28,"",3650,76.7,""],
    [1485,2013,"Borders","All major congenital conditions registerable by EUROCAT",25,"",1036,241.3,""],
    [1489,2013,"Borders","Congenital heart diseases (CHD)",8,"",1036,77.2,""],
    [1493,2013,"Borders","Abdominal wall defects",0,"",1036,0,""],
    [1497,2013,"Borders","Other conditions/syndromes",0,"",1036,0,""],
    [1499,2013,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",35,"",1309,267.4,""],
    [1500,2013,"Dumfries and Galloway","Nervous system conditions",6,"",1309,45.8,""],
    [1501,2013,"Dumfries and Galloway","Eye conditions",0,"",1309,0,""],
    [1502,2013,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1309,0,""],
    [1503,2013,"Dumfries and Galloway","Congenital heart diseases (CHD)",6,"",1309,45.8,""],
    [1508,2013,"Dumfries and Galloway","Kidney and urinary tract conditions",10,"",1309,76.4,""],
    [1513,2013,"Fife","All major congenital conditions registerable by EUROCAT",106,"",3847,275.5,""],
    [1514,2013,"Fife","Nervous system conditions",13,"",3847,33.8,""],
    [1517,2013,"Fife","Congenital heart diseases (CHD)",27,"",3847,70.2,""],
    [1520,2013,"Fife","Gastro-intestinal conditions",11,"",3847,28.6,""],
    [1521,2013,"Fife","Abdominal wall defects",5,"",3847,13,""],
    [1522,2013,"Fife","Kidney and urinary tract conditions",7,"",3847,18.2,""],
    [1523,2013,"Fife","Genital conditions",8,"",3847,20.8,""],
    [1524,2013,"Fife","Limb conditions",12,"",3847,31.2,""],
    [1525,2013,"Fife","Other conditions/syndromes",11,"",3847,28.6,""],
    [1526,2013,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",17,"",3847,44.2,""],
    [1527,2013,"Forth Valley","All major congenital conditions registerable by EUROCAT",74,"",3021,245,""],
    [1528,2013,"Forth Valley","Nervous system conditions",7,"",3021,23.2,""],
    [1529,2013,"Forth Valley","Eye conditions",0,"",3021,0,""],
    [1530,2013,"Forth Valley","Ear, face and neck conditions",0,"",3021,0,""],
    [1531,2013,"Forth Valley","Congenital heart diseases (CHD)",9,"",3021,29.8,""],
    [1532,2013,"Forth Valley","Respiratory conditions",6,"",3021,19.9,""],
    [1533,2013,"Forth Valley","Oro-facial clefts",7,"",3021,23.2,""],
    [1534,2013,"Forth Valley","Gastro-intestinal conditions",6,"",3021,19.9,""],
    [1536,2013,"Forth Valley","Kidney and urinary tract conditions",8,"",3021,26.5,""],
    [1537,2013,"Forth Valley","Genital conditions",20,"",3021,66.2,""],
    [1538,2013,"Forth Valley","Limb conditions",6,"",3021,19.9,""],
    [1539,2013,"Forth Valley","Other conditions/syndromes",5,"",3021,16.6,""],
    [1540,2013,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",5,"",3021,16.6,""],
    [1541,2013,"Grampian","All major congenital conditions registerable by EUROCAT",221,"",6164,358.5,""],
    [1542,2013,"Grampian","Nervous system conditions",25,"",6164,40.6,""],
    [1544,2013,"Grampian","Ear, face and neck conditions",0,"",6164,0,""],
    [1545,2013,"Grampian","Congenital heart diseases (CHD)",67,"",6164,108.7,""],
    [1547,2013,"Grampian","Oro-facial clefts",15,"",6164,24.3,""],
    [1548,2013,"Grampian","Gastro-intestinal conditions",11,"",6164,17.8,""],
    [1549,2013,"Grampian","Abdominal wall defects",0,"",6164,0,""],
    [1550,2013,"Grampian","Kidney and urinary tract conditions",17,"",6164,27.6,""],
    [1551,2013,"Grampian","Genital conditions",21,"",6164,34.1,""],
    [1552,2013,"Grampian","Limb conditions",37,"",6164,60,""],
    [1553,2013,"Grampian","Other conditions/syndromes",10,"",6164,16.2,""],
    [1554,2013,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",35,"",6164,56.8,""],
    [1555,2013,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",451,"",12606,357.8,""],
    [1556,2013,"Greater Glasgow and Clyde","Nervous system conditions",31,"",12606,24.6,""],
    [1557,2013,"Greater Glasgow and Clyde","Eye conditions",28,"",12606,22.2,""],
    [1559,2013,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",120,"",12606,95.2,""],
    [1560,2013,"Greater Glasgow and Clyde","Respiratory conditions",26,"",12606,20.6,""],
    [1561,2013,"Greater Glasgow and Clyde","Oro-facial clefts",11,"",12606,8.7,""],
    [1562,2013,"Greater Glasgow and Clyde","Gastro-intestinal conditions",37,"",12606,29.4,""],
    [1563,2013,"Greater Glasgow and Clyde","Abdominal wall defects",7,"",12606,5.6,""],
    [1564,2013,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",60,"",12606,47.6,""],
    [1565,2013,"Greater Glasgow and Clyde","Genital conditions",49,"",12606,38.9,""],
    [1566,2013,"Greater Glasgow and Clyde","Limb conditions",58,"",12606,46,""],
    [1567,2013,"Greater Glasgow and Clyde","Other conditions/syndromes",18,"",12606,14.3,""],
    [1568,2013,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",51,"",12606,40.5,""],
    [1569,2013,"Highland","All major congenital conditions registerable by EUROCAT",127,"",2941,431.8,""],
    [1573,2013,"Highland","Congenital heart diseases (CHD)",57,"",2941,193.8,""],
    [1575,2013,"Highland","Oro-facial clefts",9,"",2941,30.6,""],
    [1576,2013,"Highland","Gastro-intestinal conditions",10,"",2941,34,""],
    [1578,2013,"Highland","Kidney and urinary tract conditions",7,"",2941,23.8,""],
    [1579,2013,"Highland","Genital conditions",15,"",2941,51,""],
    [1580,2013,"Highland","Limb conditions",12,"",2941,40.8,""],
    [1581,2013,"Highland","Other conditions/syndromes",7,"",2941,23.8,""],
    [1582,2013,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",20,"",2941,68,""],
    [1583,2013,"Lanarkshire","All major congenital conditions registerable by EUROCAT",224,"",7020,319.1,""],
    [1584,2013,"Lanarkshire","Nervous system conditions",19,"",7020,27.1,""],
    [1585,2013,"Lanarkshire","Eye conditions",8,"",7020,11.4,""],
    [1586,2013,"Lanarkshire","Ear, face and neck conditions",0,"",7020,0,""],
    [1587,2013,"Lanarkshire","Congenital heart diseases (CHD)",69,"",7020,98.3,""],
    [1588,2013,"Lanarkshire","Respiratory conditions",7,"",7020,10,""],
    [1589,2013,"Lanarkshire","Oro-facial clefts",9,"",7020,12.8,""],
    [1590,2013,"Lanarkshire","Gastro-intestinal conditions",23,"",7020,32.8,""],
    [1592,2013,"Lanarkshire","Kidney and urinary tract conditions",24,"",7020,34.2,""],
    [1593,2013,"Lanarkshire","Genital conditions",28,"",7020,39.9,""],
    [1594,2013,"Lanarkshire","Limb conditions",23,"",7020,32.8,""],
    [1595,2013,"Lanarkshire","Other conditions/syndromes",10,"",7020,14.2,""],
    [1596,2013,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",25,"",7020,35.6,""],
    [1597,2013,"Lothian","All major congenital conditions registerable by EUROCAT",410,"",9607,426.8,""],
    [1598,2013,"Lothian","Nervous system conditions",29,"",9607,30.2,""],
    [1600,2013,"Lothian","Ear, face and neck conditions",6,"",9607,6.2,""],
    [1601,2013,"Lothian","Congenital heart diseases (CHD)",56,"",9607,58.3,""],
    [1602,2013,"Lothian","Respiratory conditions",5,"",9607,5.2,""],
    [1603,2013,"Lothian","Oro-facial clefts",18,"",9607,18.7,""],
    [1604,2013,"Lothian","Gastro-intestinal conditions",34,"",9607,35.4,""],
    [1605,2013,"Lothian","Abdominal wall defects",9,"",9607,9.4,""],
    [1606,2013,"Lothian","Kidney and urinary tract conditions",38,"",9607,39.6,""],
    [1607,2013,"Lothian","Genital conditions",63,"",9607,65.6,""],
    [1608,2013,"Lothian","Limb conditions",125,"",9607,130.1,""],
    [1609,2013,"Lothian","Other conditions/syndromes",15,"",9607,15.6,""],
    [1610,2013,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",50,"",9607,52,""],
    [1611,2013,"Orkney","All major congenital conditions registerable by EUROCAT",6,"",197,304.6,""],
    [1613,2013,"Orkney","Eye conditions",0,"",197,0,""],
    [1614,2013,"Orkney","Ear, face and neck conditions",0,"",197,0,""],
    [1616,2013,"Orkney","Respiratory conditions",0,"",197,0,""],
    [1617,2013,"Orkney","Oro-facial clefts",0,"",197,0,""],
    [1618,2013,"Orkney","Gastro-intestinal conditions",0,"",197,0,""],
    [1619,2013,"Orkney","Abdominal wall defects",0,"",197,0,""],
    [1621,2013,"Orkney","Genital conditions",0,"",197,0,""],
    [1623,2013,"Orkney","Other conditions/syndromes",0,"",197,0,""],
    [1625,2013,"Shetland","All major congenital conditions registerable by EUROCAT",5,"",252,198.4,""],
    [1626,2013,"Shetland","Nervous system conditions",0,"",252,0,""],
    [1628,2013,"Shetland","Ear, face and neck conditions",0,"",252,0,""],
    [1630,2013,"Shetland","Respiratory conditions",0,"",252,0,""],
    [1631,2013,"Shetland","Oro-facial clefts",0,"",252,0,""],
    [1633,2013,"Shetland","Abdominal wall defects",0,"",252,0,""],
    [1636,2013,"Shetland","Limb conditions",0,"",252,0,""],
    [1637,2013,"Shetland","Other conditions/syndromes",0,"",252,0,""],
    [1639,2013,"Tayside","All major congenital conditions registerable by EUROCAT",107,"",4035,265.2,""],
    [1640,2013,"Tayside","Nervous system conditions",12,"",4035,29.7,""],
    [1641,2013,"Tayside","Eye conditions",0,"",4035,0,""],
    [1643,2013,"Tayside","Congenital heart diseases (CHD)",22,"",4035,54.5,""],
    [1645,2013,"Tayside","Oro-facial clefts",7,"",4035,17.3,""],
    [1647,2013,"Tayside","Abdominal wall defects",5,"",4035,12.4,""],
    [1648,2013,"Tayside","Kidney and urinary tract conditions",7,"",4035,17.3,""],
    [1649,2013,"Tayside","Genital conditions",19,"",4035,47.1,""],
    [1650,2013,"Tayside","Limb conditions",15,"",4035,37.2,""],
    [1651,2013,"Tayside","Other conditions/syndromes",7,"",4035,17.3,""],
    [1652,2013,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",19,"",4035,47.1,""],
    [1653,2013,"Total","All major congenital conditions registerable by EUROCAT",1942,"",56135,346,""],
    [1654,2013,"Total","Nervous system conditions",158,"",56135,28.1,""],
    [1655,2013,"Total","Eye conditions",49,"",56135,8.7,""],
    [1656,2013,"Total","Ear, face and neck conditions",13,"",56135,2.3,""],
    [1657,2013,"Total","Congenital heart diseases (CHD)",487,"",56135,86.8,""],
    [1658,2013,"Total","Respiratory conditions",58,"",56135,10.3,""],
    [1659,2013,"Total","Oro-facial clefts",93,"",56135,16.6,""],
    [1660,2013,"Total","Gastro-intestinal conditions",157,"",56135,28,""],
    [1661,2013,"Total","Abdominal wall defects",39,"",56135,6.9,""],
    [1662,2013,"Total","Kidney and urinary tract conditions",198,"",56135,35.3,""],
    [1663,2013,"Total","Genital conditions",245,"",56135,43.6,""],
    [1664,2013,"Total","Limb conditions",323,"",56135,57.5,""],
    [1665,2013,"Total","Other conditions/syndromes",91,"",56135,16.2,""],
    [1666,2013,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",262,"",56135,46.7,""],
    [1667,2013,"Western Isles","All major congenital conditions registerable by EUROCAT",7,"",251,278.9,""],
    [1668,2013,"Western Isles","Nervous system conditions",0,"",251,0,""],
    [1669,2013,"Western Isles","Eye conditions",0,"",251,0,""],
    [1670,2013,"Western Isles","Ear, face and neck conditions",0,"",251,0,""],
    [1673,2013,"Western Isles","Oro-facial clefts",0,"",251,0,""],
    [1675,2013,"Western Isles","Abdominal wall defects",0,"",251,0,""],
    [1677,2013,"Western Isles","Genital conditions",0,"",251,0,""],
    [1679,2013,"Western Isles","Other conditions/syndromes",0,"",251,0,""],
    [1681,2012,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",125,"",3721,335.9,""],
    [1682,2012,"Ayrshire and Arran","Nervous system conditions",10,"",3721,26.9,""],
    [1684,2012,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3721,0,""],
    [1685,2012,"Ayrshire and Arran","Congenital heart diseases (CHD)",40,"",3721,107.5,""],
    [1687,2012,"Ayrshire and Arran","Oro-facial clefts",5,"",3721,13.4,""],
    [1688,2012,"Ayrshire and Arran","Gastro-intestinal conditions",7,"",3721,18.8,""],
    [1689,2012,"Ayrshire and Arran","Abdominal wall defects",0,"",3721,0,""],
    [1690,2012,"Ayrshire and Arran","Kidney and urinary tract conditions",18,"",3721,48.4,""],
    [1691,2012,"Ayrshire and Arran","Genital conditions",16,"",3721,43,""],
    [1692,2012,"Ayrshire and Arran","Limb conditions",16,"",3721,43,""],
    [1694,2012,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",3721,43,""],
    [1695,2012,"Borders","All major congenital conditions registerable by EUROCAT",18,"",1027,175.3,""],
    [1697,2012,"Borders","Eye conditions",0,"",1027,0,""],
    [1698,2012,"Borders","Ear, face and neck conditions",0,"",1027,0,""],
    [1699,2012,"Borders","Congenital heart diseases (CHD)",6,"",1027,58.4,""],
    [1700,2012,"Borders","Respiratory conditions",0,"",1027,0,""],
    [1701,2012,"Borders","Oro-facial clefts",0,"",1027,0,""],
    [1703,2012,"Borders","Abdominal wall defects",0,"",1027,0,""],
    [1704,2012,"Borders","Kidney and urinary tract conditions",0,"",1027,0,""],
    [1709,2012,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",46,"",1395,329.7,""],
    [1713,2012,"Dumfries and Galloway","Congenital heart diseases (CHD)",13,"",1395,93.2,""],
    [1717,2012,"Dumfries and Galloway","Abdominal wall defects",0,"",1395,0,""],
    [1719,2012,"Dumfries and Galloway","Genital conditions",7,"",1395,50.2,""],
    [1721,2012,"Dumfries and Galloway","Other conditions/syndromes",0,"",1395,0,""],
    [1722,2012,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",7,"",1395,50.2,""],
    [1723,2012,"Fife","All major congenital conditions registerable by EUROCAT",113,"",4064,278.1,""],
    [1724,2012,"Fife","Nervous system conditions",17,"",4064,41.8,""],
    [1727,2012,"Fife","Congenital heart diseases (CHD)",28,"",4064,68.9,""],
    [1729,2012,"Fife","Oro-facial clefts",6,"",4064,14.8,""],
    [1730,2012,"Fife","Gastro-intestinal conditions",10,"",4064,24.6,""],
    [1732,2012,"Fife","Kidney and urinary tract conditions",8,"",4064,19.7,""],
    [1733,2012,"Fife","Genital conditions",10,"",4064,24.6,""],
    [1734,2012,"Fife","Limb conditions",8,"",4064,19.7,""],
    [1736,2012,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",26,"",4064,64,""],
    [1737,2012,"Forth Valley","All major congenital conditions registerable by EUROCAT",97,"",3232,300.1,""],
    [1738,2012,"Forth Valley","Nervous system conditions",11,"",3232,34,""],
    [1740,2012,"Forth Valley","Ear, face and neck conditions",0,"",3232,0,""],
    [1741,2012,"Forth Valley","Congenital heart diseases (CHD)",19,"",3232,58.8,""],
    [1743,2012,"Forth Valley","Oro-facial clefts",11,"",3232,34,""],
    [1744,2012,"Forth Valley","Gastro-intestinal conditions",14,"",3232,43.3,""],
    [1746,2012,"Forth Valley","Kidney and urinary tract conditions",7,"",3232,21.7,""],
    [1747,2012,"Forth Valley","Genital conditions",9,"",3232,27.8,""],
    [1748,2012,"Forth Valley","Limb conditions",13,"",3232,40.2,""],
    [1750,2012,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",23,"",3232,71.2,""],
    [1751,2012,"Grampian","All major congenital conditions registerable by EUROCAT",252,"",6508,387.2,""],
    [1752,2012,"Grampian","Nervous system conditions",26,"",6508,40,""],
    [1755,2012,"Grampian","Congenital heart diseases (CHD)",70,"",6508,107.6,""],
    [1757,2012,"Grampian","Oro-facial clefts",10,"",6508,15.4,""],
    [1758,2012,"Grampian","Gastro-intestinal conditions",13,"",6508,20,""],
    [1759,2012,"Grampian","Abdominal wall defects",8,"",6508,12.3,""],
    [1760,2012,"Grampian","Kidney and urinary tract conditions",19,"",6508,29.2,""],
    [1761,2012,"Grampian","Genital conditions",26,"",6508,40,""],
    [1762,2012,"Grampian","Limb conditions",49,"",6508,75.3,""],
    [1763,2012,"Grampian","Other conditions/syndromes",8,"",6508,12.3,""],
    [1764,2012,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",52,"",6508,79.9,""],
    [1765,2012,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",397,"",13128,302.4,""],
    [1766,2012,"Greater Glasgow and Clyde","Nervous system conditions",25,"",13128,19,""],
    [1767,2012,"Greater Glasgow and Clyde","Eye conditions",15,"",13128,11.4,""],
    [1769,2012,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",116,"",13128,88.4,""],
    [1770,2012,"Greater Glasgow and Clyde","Respiratory conditions",18,"",13128,13.7,""],
    [1771,2012,"Greater Glasgow and Clyde","Oro-facial clefts",15,"",13128,11.4,""],
    [1772,2012,"Greater Glasgow and Clyde","Gastro-intestinal conditions",35,"",13128,26.7,""],
    [1773,2012,"Greater Glasgow and Clyde","Abdominal wall defects",8,"",13128,6.1,""],
    [1774,2012,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",26,"",13128,19.8,""],
    [1775,2012,"Greater Glasgow and Clyde","Genital conditions",40,"",13128,30.5,""],
    [1776,2012,"Greater Glasgow and Clyde","Limb conditions",52,"",13128,39.6,""],
    [1777,2012,"Greater Glasgow and Clyde","Other conditions/syndromes",24,"",13128,18.3,""],
    [1778,2012,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",51,"",13128,38.8,""],
    [1779,2012,"Highland","All major congenital conditions registerable by EUROCAT",116,"",3152,368,""],
    [1780,2012,"Highland","Nervous system conditions",8,"",3152,25.4,""],
    [1782,2012,"Highland","Ear, face and neck conditions",0,"",3152,0,""],
    [1783,2012,"Highland","Congenital heart diseases (CHD)",56,"",3152,177.7,""],
    [1786,2012,"Highland","Gastro-intestinal conditions",5,"",3152,15.9,""],
    [1789,2012,"Highland","Genital conditions",12,"",3152,38.1,""],
    [1790,2012,"Highland","Limb conditions",16,"",3152,50.8,""],
    [1792,2012,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",3152,47.6,""],
    [1793,2012,"Lanarkshire","All major congenital conditions registerable by EUROCAT",230,"",7153,321.5,""],
    [1794,2012,"Lanarkshire","Nervous system conditions",25,"",7153,35,""],
    [1796,2012,"Lanarkshire","Ear, face and neck conditions",0,"",7153,0,""],
    [1797,2012,"Lanarkshire","Congenital heart diseases (CHD)",54,"",7153,75.5,""],
    [1798,2012,"Lanarkshire","Respiratory conditions",17,"",7153,23.8,""],
    [1799,2012,"Lanarkshire","Oro-facial clefts",13,"",7153,18.2,""],
    [1800,2012,"Lanarkshire","Gastro-intestinal conditions",13,"",7153,18.2,""],
    [1801,2012,"Lanarkshire","Abdominal wall defects",6,"",7153,8.4,""],
    [1802,2012,"Lanarkshire","Kidney and urinary tract conditions",18,"",7153,25.2,""],
    [1803,2012,"Lanarkshire","Genital conditions",20,"",7153,28,""],
    [1804,2012,"Lanarkshire","Limb conditions",25,"",7153,35,""],
    [1805,2012,"Lanarkshire","Other conditions/syndromes",11,"",7153,15.4,""],
    [1806,2012,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",34,"",7153,47.5,""],
    [1807,2012,"Lothian","All major congenital conditions registerable by EUROCAT",396,"",9839,402.5,""],
    [1808,2012,"Lothian","Nervous system conditions",32,"",9839,32.5,""],
    [1809,2012,"Lothian","Eye conditions",11,"",9839,11.2,""],
    [1810,2012,"Lothian","Ear, face and neck conditions",9,"",9839,9.1,""],
    [1811,2012,"Lothian","Congenital heart diseases (CHD)",66,"",9839,67.1,""],
    [1813,2012,"Lothian","Oro-facial clefts",18,"",9839,18.3,""],
    [1814,2012,"Lothian","Gastro-intestinal conditions",41,"",9839,41.7,""],
    [1815,2012,"Lothian","Abdominal wall defects",7,"",9839,7.1,""],
    [1816,2012,"Lothian","Kidney and urinary tract conditions",30,"",9839,30.5,""],
    [1817,2012,"Lothian","Genital conditions",60,"",9839,61,""],
    [1818,2012,"Lothian","Limb conditions",93,"",9839,94.5,""],
    [1819,2012,"Lothian","Other conditions/syndromes",15,"",9839,15.2,""],
    [1820,2012,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",70,"",9839,71.1,""],
    [1821,2012,"Orkney","All major congenital conditions registerable by EUROCAT",9,"",205,439,""],
    [1823,2012,"Orkney","Eye conditions",0,"",205,0,""],
    [1824,2012,"Orkney","Ear, face and neck conditions",0,"",205,0,""],
    [1826,2012,"Orkney","Respiratory conditions",0,"",205,0,""],
    [1828,2012,"Orkney","Gastro-intestinal conditions",0,"",205,0,""],
    [1829,2012,"Orkney","Abdominal wall defects",0,"",205,0,""],
    [1831,2012,"Orkney","Genital conditions",0,"",205,0,""],
    [1833,2012,"Orkney","Other conditions/syndromes",0,"",205,0,""],
    [1835,2012,"Shetland","All major congenital conditions registerable by EUROCAT",12,"",279,430.1,""],
    [1837,2012,"Shetland","Eye conditions",0,"",279,0,""],
    [1838,2012,"Shetland","Ear, face and neck conditions",0,"",279,0,""],
    [1840,2012,"Shetland","Respiratory conditions",0,"",279,0,""],
    [1842,2012,"Shetland","Gastro-intestinal conditions",0,"",279,0,""],
    [1843,2012,"Shetland","Abdominal wall defects",0,"",279,0,""],
    [1847,2012,"Shetland","Other conditions/syndromes",0,"",279,0,""],
    [1849,2012,"Tayside","All major congenital conditions registerable by EUROCAT",119,"",4135,287.8,""],
    [1850,2012,"Tayside","Nervous system conditions",11,"",4135,26.6,""],
    [1853,2012,"Tayside","Congenital heart diseases (CHD)",20,"",4135,48.4,""],
    [1855,2012,"Tayside","Oro-facial clefts",9,"",4135,21.8,""],
    [1856,2012,"Tayside","Gastro-intestinal conditions",9,"",4135,21.8,""],
    [1859,2012,"Tayside","Genital conditions",34,"",4135,82.2,""],
    [1860,2012,"Tayside","Limb conditions",14,"",4135,33.9,""],
    [1862,2012,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",4135,38.7,""],
    [1863,2012,"Total","All major congenital conditions registerable by EUROCAT",1939,"",58310,332.5,""],
    [1864,2012,"Total","Nervous system conditions",175,"",58310,30,""],
    [1865,2012,"Total","Eye conditions",44,"",58310,7.5,""],
    [1866,2012,"Total","Ear, face and neck conditions",16,"",58310,2.7,""],
    [1867,2012,"Total","Congenital heart diseases (CHD)",495,"",58310,84.9,""],
    [1868,2012,"Total","Respiratory conditions",55,"",58310,9.4,""],
    [1869,2012,"Total","Oro-facial clefts",92,"",58310,15.8,""],
    [1870,2012,"Total","Gastro-intestinal conditions",152,"",58310,26.1,""],
    [1871,2012,"Total","Abdominal wall defects",37,"",58310,6.3,""],
    [1872,2012,"Total","Kidney and urinary tract conditions",142,"",58310,24.4,""],
    [1873,2012,"Total","Genital conditions",239,"",58310,41,""],
    [1874,2012,"Total","Limb conditions",295,"",58310,50.6,""],
    [1875,2012,"Total","Other conditions/syndromes",77,"",58310,13.2,""],
    [1876,2012,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",321,"",58310,55.1,""],
    [1877,2012,"Western Isles","All major congenital conditions registerable by EUROCAT",5,"",234,213.7,""],
    [1879,2012,"Western Isles","Eye conditions",0,"",234,0,""],
    [1880,2012,"Western Isles","Ear, face and neck conditions",0,"",234,0,""],
    [1882,2012,"Western Isles","Respiratory conditions",0,"",234,0,""],
    [1883,2012,"Western Isles","Oro-facial clefts",0,"",234,0,""],
    [1884,2012,"Western Isles","Gastro-intestinal conditions",0,"",234,0,""],
    [1885,2012,"Western Isles","Abdominal wall defects",0,"",234,0,""],
    [1886,2012,"Western Isles","Kidney and urinary tract conditions",0,"",234,0,""],
    [1888,2012,"Western Isles","Limb conditions",0,"",234,0,""],
    [1889,2012,"Western Isles","Other conditions/syndromes",0,"",234,0,""],
    [1891,2011,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",124,"",3888,318.9,""],
    [1892,2011,"Ayrshire and Arran","Nervous system conditions",14,"",3888,36,""],
    [1895,2011,"Ayrshire and Arran","Congenital heart diseases (CHD)",28,"",3888,72,""],
    [1897,2011,"Ayrshire and Arran","Oro-facial clefts",10,"",3888,25.7,""],
    [1898,2011,"Ayrshire and Arran","Gastro-intestinal conditions",10,"",3888,25.7,""],
    [1900,2011,"Ayrshire and Arran","Kidney and urinary tract conditions",14,"",3888,36,""],
    [1901,2011,"Ayrshire and Arran","Genital conditions",19,"",3888,48.9,""],
    [1902,2011,"Ayrshire and Arran","Limb conditions",20,"",3888,51.4,""],
    [1904,2011,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",3888,38.6,""],
    [1905,2011,"Borders","All major congenital conditions registerable by EUROCAT",26,"",1021,254.7,""],
    [1907,2011,"Borders","Eye conditions",0,"",1021,0,""],
    [1909,2011,"Borders","Congenital heart diseases (CHD)",9,"",1021,88.1,""],
    [1919,2011,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",42,"",1386,303,""],
    [1923,2011,"Dumfries and Galloway","Congenital heart diseases (CHD)",10,"",1386,72.2,""],
    [1925,2011,"Dumfries and Galloway","Oro-facial clefts",0,"",1386,0,""],
    [1926,2011,"Dumfries and Galloway","Gastro-intestinal conditions",5,"",1386,36.1,""],
    [1928,2011,"Dumfries and Galloway","Kidney and urinary tract conditions",7,"",1386,50.5,""],
    [1932,2011,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",12,"",1386,86.6,""],
    [1933,2011,"Fife","All major congenital conditions registerable by EUROCAT",101,"",4190,241.1,""],
    [1934,2011,"Fife","Nervous system conditions",19,"",4190,45.3,""],
    [1937,2011,"Fife","Congenital heart diseases (CHD)",22,"",4190,52.5,""],
    [1939,2011,"Fife","Oro-facial clefts",7,"",4190,16.7,""],
    [1940,2011,"Fife","Gastro-intestinal conditions",5,"",4190,11.9,""],
    [1942,2011,"Fife","Kidney and urinary tract conditions",12,"",4190,28.6,""],
    [1943,2011,"Fife","Genital conditions",7,"",4190,16.7,""],
    [1944,2011,"Fife","Limb conditions",13,"",4190,31,""],
    [1945,2011,"Fife","Other conditions/syndromes",7,"",4190,16.7,""],
    [1946,2011,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",17,"",4190,40.6,""],
    [1947,2011,"Forth Valley","All major congenital conditions registerable by EUROCAT",74,"",3203,231,""],
    [1948,2011,"Forth Valley","Nervous system conditions",7,"",3203,21.9,""],
    [1951,2011,"Forth Valley","Congenital heart diseases (CHD)",21,"",3203,65.6,""],
    [1954,2011,"Forth Valley","Gastro-intestinal conditions",9,"",3203,28.1,""],
    [1957,2011,"Forth Valley","Genital conditions",8,"",3203,25,""],
    [1958,2011,"Forth Valley","Limb conditions",10,"",3203,31.2,""],
    [1960,2011,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",13,"",3203,40.6,""],
    [1961,2011,"Grampian","All major congenital conditions registerable by EUROCAT",240,"",6297,381.1,""],
    [1962,2011,"Grampian","Nervous system conditions",24,"",6297,38.1,""],
    [1965,2011,"Grampian","Congenital heart diseases (CHD)",70,"",6297,111.2,""],
    [1967,2011,"Grampian","Oro-facial clefts",8,"",6297,12.7,""],
    [1968,2011,"Grampian","Gastro-intestinal conditions",11,"",6297,17.5,""],
    [1970,2011,"Grampian","Kidney and urinary tract conditions",17,"",6297,27,""],
    [1971,2011,"Grampian","Genital conditions",27,"",6297,42.9,""],
    [1972,2011,"Grampian","Limb conditions",29,"",6297,46.1,""],
    [1973,2011,"Grampian","Other conditions/syndromes",10,"",6297,15.9,""],
    [1974,2011,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",49,"",6297,77.8,""],
    [1975,2011,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",394,"",13196,298.6,""],
    [1976,2011,"Greater Glasgow and Clyde","Nervous system conditions",23,"",13196,17.4,""],
    [1977,2011,"Greater Glasgow and Clyde","Eye conditions",11,"",13196,8.3,""],
    [1979,2011,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",104,"",13196,78.8,""],
    [1980,2011,"Greater Glasgow and Clyde","Respiratory conditions",30,"",13196,22.7,""],
    [1981,2011,"Greater Glasgow and Clyde","Oro-facial clefts",24,"",13196,18.2,""],
    [1982,2011,"Greater Glasgow and Clyde","Gastro-intestinal conditions",44,"",13196,33.3,""],
    [1984,2011,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",35,"",13196,26.5,""],
    [1985,2011,"Greater Glasgow and Clyde","Genital conditions",48,"",13196,36.4,""],
    [1986,2011,"Greater Glasgow and Clyde","Limb conditions",48,"",13196,36.4,""],
    [1987,2011,"Greater Glasgow and Clyde","Other conditions/syndromes",22,"",13196,16.7,""],
    [1988,2011,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",65,"",13196,49.3,""],
    [1989,2011,"Highland","All major congenital conditions registerable by EUROCAT",175,"",3097,565.1,""],
    [1990,2011,"Highland","Nervous system conditions",12,"",3097,38.7,""],
    [1993,2011,"Highland","Congenital heart diseases (CHD)",107,"",3097,345.5,""],
    [1996,2011,"Highland","Gastro-intestinal conditions",6,"",3097,19.4,""],
    [1997,2011,"Highland","Abdominal wall defects",5,"",3097,16.1,""],
    [1999,2011,"Highland","Genital conditions",14,"",3097,45.2,""],
    [2000,2011,"Highland","Limb conditions",20,"",3097,64.6,""],
    [2002,2011,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",14,"",3097,45.2,""],
    [2003,2011,"Lanarkshire","All major congenital conditions registerable by EUROCAT",200,"",7463,268,""],
    [2004,2011,"Lanarkshire","Nervous system conditions",15,"",7463,20.1,""],
    [2005,2011,"Lanarkshire","Eye conditions",7,"",7463,9.4,""],
    [2007,2011,"Lanarkshire","Congenital heart diseases (CHD)",39,"",7463,52.3,""],
    [2008,2011,"Lanarkshire","Respiratory conditions",5,"",7463,6.7,""],
    [2009,2011,"Lanarkshire","Oro-facial clefts",15,"",7463,20.1,""],
    [2010,2011,"Lanarkshire","Gastro-intestinal conditions",22,"",7463,29.5,""],
    [2012,2011,"Lanarkshire","Kidney and urinary tract conditions",28,"",7463,37.5,""],
    [2013,2011,"Lanarkshire","Genital conditions",27,"",7463,36.2,""],
    [2014,2011,"Lanarkshire","Limb conditions",19,"",7463,25.5,""],
    [2015,2011,"Lanarkshire","Other conditions/syndromes",12,"",7463,16.1,""],
    [2016,2011,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",27,"",7463,36.2,""],
    [2017,2011,"Lothian","All major congenital conditions registerable by EUROCAT",370,"",9856,375.4,""],
    [2018,2011,"Lothian","Nervous system conditions",33,"",9856,33.5,""],
    [2019,2011,"Lothian","Eye conditions",8,"",9856,8.1,""],
    [2021,2011,"Lothian","Congenital heart diseases (CHD)",63,"",9856,63.9,""],
    [2022,2011,"Lothian","Respiratory conditions",12,"",9856,12.2,""],
    [2023,2011,"Lothian","Oro-facial clefts",7,"",9856,7.1,""],
    [2024,2011,"Lothian","Gastro-intestinal conditions",26,"",9856,26.4,""],
    [2025,2011,"Lothian","Abdominal wall defects",6,"",9856,6.1,""],
    [2026,2011,"Lothian","Kidney and urinary tract conditions",30,"",9856,30.4,""],
    [2027,2011,"Lothian","Genital conditions",63,"",9856,63.9,""],
    [2028,2011,"Lothian","Limb conditions",76,"",9856,77.1,""],
    [2029,2011,"Lothian","Other conditions/syndromes",8,"",9856,8.1,""],
    [2030,2011,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",55,"",9856,55.8,""],
    [2033,2011,"Orkney","Eye conditions",0,"",201,0,""],
    [2036,2011,"Orkney","Respiratory conditions",0,"",201,0,""],
    [2038,2011,"Orkney","Gastro-intestinal conditions",0,"",201,0,""],
    [2039,2011,"Orkney","Abdominal wall defects",0,"",201,0,""],
    [2040,2011,"Orkney","Kidney and urinary tract conditions",0,"",201,0,""],
    [2042,2011,"Orkney","Limb conditions",0,"",201,0,""],
    [2043,2011,"Orkney","Other conditions/syndromes",0,"",201,0,""],
    [2045,2011,"Shetland","All major congenital conditions registerable by EUROCAT",11,"",250,440,""],
    [2046,2011,"Shetland","Nervous system conditions",0,"",250,0,""],
    [2047,2011,"Shetland","Eye conditions",0,"",250,0,""],
    [2050,2011,"Shetland","Respiratory conditions",0,"",250,0,""],
    [2054,2011,"Shetland","Kidney and urinary tract conditions",0,"",250,0,""],
    [2056,2011,"Shetland","Limb conditions",0,"",250,0,""],
    [2057,2011,"Shetland","Other conditions/syndromes",0,"",250,0,""],
    [2058,2011,"Shetland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",5,"",250,200,""],
    [2059,2011,"Tayside","All major congenital conditions registerable by EUROCAT",98,"",4402,222.6,""],
    [2060,2011,"Tayside","Nervous system conditions",7,"",4402,15.9,""],
    [2063,2011,"Tayside","Congenital heart diseases (CHD)",15,"",4402,34.1,""],
    [2065,2011,"Tayside","Oro-facial clefts",9,"",4402,20.4,""],
    [2066,2011,"Tayside","Gastro-intestinal conditions",7,"",4402,15.9,""],
    [2069,2011,"Tayside","Genital conditions",20,"",4402,45.4,""],
    [2070,2011,"Tayside","Limb conditions",12,"",4402,27.3,""],
    [2072,2011,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",4402,36.3,""],
    [2073,2011,"Total","All major congenital conditions registerable by EUROCAT",1868,"",58924,317,""],
    [2074,2011,"Total","Nervous system conditions",161,"",58924,27.3,""],
    [2075,2011,"Total","Eye conditions",43,"",58924,7.3,""],
    [2076,2011,"Total","Ear, face and neck conditions",3,"",58924,0.5,""],
    [2077,2011,"Total","Congenital heart diseases (CHD)",494,"",58924,83.8,""],
    [2078,2011,"Total","Respiratory conditions",62,"",58924,10.5,""],
    [2079,2011,"Total","Oro-facial clefts",91,"",58924,15.4,""],
    [2080,2011,"Total","Gastro-intestinal conditions",150,"",58924,25.5,""],
    [2081,2011,"Total","Abdominal wall defects",31,"",58924,5.3,""],
    [2082,2011,"Total","Kidney and urinary tract conditions",157,"",58924,26.6,""],
    [2083,2011,"Total","Genital conditions",242,"",58924,41.1,""],
    [2084,2011,"Total","Limb conditions",254,"",58924,43.1,""],
    [2085,2011,"Total","Other conditions/syndromes",76,"",58924,12.9,""],
    [2086,2011,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",293,"",58924,49.7,""],
    [2087,2011,"Western Isles","All major congenital conditions registerable by EUROCAT",6,"",235,255.3,""],
    [2089,2011,"Western Isles","Eye conditions",0,"",235,0,""],
    [2092,2011,"Western Isles","Respiratory conditions",0,"",235,0,""],
    [2095,2011,"Western Isles","Abdominal wall defects",0,"",235,0,""],
    [2096,2011,"Western Isles","Kidney and urinary tract conditions",0,"",235,0,""],
    [2097,2011,"Western Isles","Genital conditions",0,"",235,0,""],
    [2099,2011,"Western Isles","Other conditions/syndromes",0,"",235,0,""],
    [2100,2011,"Western Isles","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",235,0,""],
    [2101,2010,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",132,"",3858,342.1,""],
    [2102,2010,"Ayrshire and Arran","Nervous system conditions",15,"",3858,38.9,""],
    [2105,2010,"Ayrshire and Arran","Congenital heart diseases (CHD)",38,"",3858,98.5,""],
    [2107,2010,"Ayrshire and Arran","Oro-facial clefts",6,"",3858,15.6,""],
    [2108,2010,"Ayrshire and Arran","Gastro-intestinal conditions",9,"",3858,23.3,""],
    [2110,2010,"Ayrshire and Arran","Kidney and urinary tract conditions",15,"",3858,38.9,""],
    [2111,2010,"Ayrshire and Arran","Genital conditions",9,"",3858,23.3,""],
    [2112,2010,"Ayrshire and Arran","Limb conditions",18,"",3858,46.7,""],
    [2113,2010,"Ayrshire and Arran","Other conditions/syndromes",8,"",3858,20.7,""],
    [2114,2010,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",3858,41.5,""],
    [2115,2010,"Borders","All major congenital conditions registerable by EUROCAT",22,"",1078,204.1,""],
    [2117,2010,"Borders","Eye conditions",0,"",1078,0,""],
    [2120,2010,"Borders","Respiratory conditions",0,"",1078,0,""],
    [2121,2010,"Borders","Oro-facial clefts",0,"",1078,0,""],
    [2122,2010,"Borders","Gastro-intestinal conditions",5,"",1078,46.4,""],
    [2128,2010,"Borders","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",7,"",1078,64.9,""],
    [2129,2010,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",50,"",1441,347,""],
    [2130,2010,"Dumfries and Galloway","Nervous system conditions",8,"",1441,55.5,""],
    [2131,2010,"Dumfries and Galloway","Eye conditions",6,"",1441,41.6,""],
    [2132,2010,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1441,0,""],
    [2133,2010,"Dumfries and Galloway","Congenital heart diseases (CHD)",7,"",1441,48.6,""],
    [2135,2010,"Dumfries and Galloway","Oro-facial clefts",0,"",1441,0,""],
    [2138,2010,"Dumfries and Galloway","Kidney and urinary tract conditions",7,"",1441,48.6,""],
    [2140,2010,"Dumfries and Galloway","Limb conditions",8,"",1441,55.5,""],
    [2142,2010,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",7,"",1441,48.6,""],
    [2143,2010,"Fife","All major congenital conditions registerable by EUROCAT",97,"",4224,229.6,""],
    [2144,2010,"Fife","Nervous system conditions",13,"",4224,30.8,""],
    [2147,2010,"Fife","Congenital heart diseases (CHD)",18,"",4224,42.6,""],
    [2148,2010,"Fife","Respiratory conditions",6,"",4224,14.2,""],
    [2149,2010,"Fife","Oro-facial clefts",14,"",4224,33.1,""],
    [2150,2010,"Fife","Gastro-intestinal conditions",6,"",4224,14.2,""],
    [2152,2010,"Fife","Kidney and urinary tract conditions",9,"",4224,21.3,""],
    [2153,2010,"Fife","Genital conditions",11,"",4224,26,""],
    [2154,2010,"Fife","Limb conditions",10,"",4224,23.7,""],
    [2156,2010,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",18,"",4224,42.6,""],
    [2157,2010,"Forth Valley","All major congenital conditions registerable by EUROCAT",72,"",3322,216.7,""],
    [2158,2010,"Forth Valley","Nervous system conditions",9,"",3322,27.1,""],
    [2159,2010,"Forth Valley","Eye conditions",0,"",3322,0,""],
    [2161,2010,"Forth Valley","Congenital heart diseases (CHD)",21,"",3322,63.2,""],
    [2164,2010,"Forth Valley","Gastro-intestinal conditions",6,"",3322,18.1,""],
    [2167,2010,"Forth Valley","Genital conditions",8,"",3322,24.1,""],
    [2168,2010,"Forth Valley","Limb conditions",7,"",3322,21.1,""],
    [2170,2010,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",3322,45.2,""],
    [2171,2010,"Grampian","All major congenital conditions registerable by EUROCAT",199,"",6254,318.2,""],
    [2172,2010,"Grampian","Nervous system conditions",17,"",6254,27.2,""],
    [2175,2010,"Grampian","Congenital heart diseases (CHD)",51,"",6254,81.5,""],
    [2177,2010,"Grampian","Oro-facial clefts",8,"",6254,12.8,""],
    [2178,2010,"Grampian","Gastro-intestinal conditions",14,"",6254,22.4,""],
    [2180,2010,"Grampian","Kidney and urinary tract conditions",19,"",6254,30.4,""],
    [2181,2010,"Grampian","Genital conditions",15,"",6254,24,""],
    [2182,2010,"Grampian","Limb conditions",30,"",6254,48,""],
    [2184,2010,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",51,"",6254,81.5,""],
    [2185,2010,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",413,"",13160,313.8,""],
    [2186,2010,"Greater Glasgow and Clyde","Nervous system conditions",30,"",13160,22.8,""],
    [2187,2010,"Greater Glasgow and Clyde","Eye conditions",8,"",13160,6.1,""],
    [2189,2010,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",97,"",13160,73.7,""],
    [2190,2010,"Greater Glasgow and Clyde","Respiratory conditions",16,"",13160,12.2,""],
    [2191,2010,"Greater Glasgow and Clyde","Oro-facial clefts",22,"",13160,16.7,""],
    [2192,2010,"Greater Glasgow and Clyde","Gastro-intestinal conditions",45,"",13160,34.2,""],
    [2193,2010,"Greater Glasgow and Clyde","Abdominal wall defects",13,"",13160,9.9,""],
    [2194,2010,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",49,"",13160,37.2,""],
    [2195,2010,"Greater Glasgow and Clyde","Genital conditions",50,"",13160,38,""],
    [2196,2010,"Greater Glasgow and Clyde","Limb conditions",53,"",13160,40.3,""],
    [2197,2010,"Greater Glasgow and Clyde","Other conditions/syndromes",22,"",13160,16.7,""],
    [2198,2010,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",47,"",13160,35.7,""],
    [2199,2010,"Highland","All major congenital conditions registerable by EUROCAT",114,"",3215,354.6,""],
    [2200,2010,"Highland","Nervous system conditions",10,"",3215,31.1,""],
    [2203,2010,"Highland","Congenital heart diseases (CHD)",51,"",3215,158.6,""],
    [2205,2010,"Highland","Oro-facial clefts",6,"",3215,18.7,""],
    [2206,2010,"Highland","Gastro-intestinal conditions",6,"",3215,18.7,""],
    [2208,2010,"Highland","Kidney and urinary tract conditions",5,"",3215,15.6,""],
    [2209,2010,"Highland","Genital conditions",7,"",3215,21.8,""],
    [2210,2010,"Highland","Limb conditions",11,"",3215,34.2,""],
    [2212,2010,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",21,"",3215,65.3,""],
    [2213,2010,"Lanarkshire","All major congenital conditions registerable by EUROCAT",231,"",7453,309.9,""],
    [2214,2010,"Lanarkshire","Nervous system conditions",17,"",7453,22.8,""],
    [2217,2010,"Lanarkshire","Congenital heart diseases (CHD)",69,"",7453,92.6,""],
    [2219,2010,"Lanarkshire","Oro-facial clefts",15,"",7453,20.1,""],
    [2220,2010,"Lanarkshire","Gastro-intestinal conditions",24,"",7453,32.2,""],
    [2222,2010,"Lanarkshire","Kidney and urinary tract conditions",20,"",7453,26.8,""],
    [2223,2010,"Lanarkshire","Genital conditions",24,"",7453,32.2,""],
    [2224,2010,"Lanarkshire","Limb conditions",25,"",7453,33.5,""],
    [2225,2010,"Lanarkshire","Other conditions/syndromes",8,"",7453,10.7,""],
    [2226,2010,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",37,"",7453,49.6,""],
    [2227,2010,"Lothian","All major congenital conditions registerable by EUROCAT",372,"",9878,376.6,""],
    [2228,2010,"Lothian","Nervous system conditions",32,"",9878,32.4,""],
    [2229,2010,"Lothian","Eye conditions",10,"",9878,10.1,""],
    [2231,2010,"Lothian","Congenital heart diseases (CHD)",55,"",9878,55.7,""],
    [2233,2010,"Lothian","Oro-facial clefts",21,"",9878,21.3,""],
    [2234,2010,"Lothian","Gastro-intestinal conditions",23,"",9878,23.3,""],
    [2235,2010,"Lothian","Abdominal wall defects",5,"",9878,5.1,""],
    [2236,2010,"Lothian","Kidney and urinary tract conditions",20,"",9878,20.2,""],
    [2237,2010,"Lothian","Genital conditions",61,"",9878,61.8,""],
    [2238,2010,"Lothian","Limb conditions",109,"",9878,110.3,""],
    [2239,2010,"Lothian","Other conditions/syndromes",14,"",9878,14.2,""],
    [2240,2010,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",49,"",9878,49.6,""],
    [2241,2010,"Orkney","All major congenital conditions registerable by EUROCAT",5,"",199,251.3,""],
    [2242,2010,"Orkney","Nervous system conditions",0,"",199,0,""],
    [2243,2010,"Orkney","Eye conditions",0,"",199,0,""],
    [2244,2010,"Orkney","Ear, face and neck conditions",0,"",199,0,""],
    [2246,2010,"Orkney","Respiratory conditions",0,"",199,0,""],
    [2248,2010,"Orkney","Gastro-intestinal conditions",0,"",199,0,""],
    [2249,2010,"Orkney","Abdominal wall defects",0,"",199,0,""],
    [2253,2010,"Orkney","Other conditions/syndromes",0,"",199,0,""],
    [2255,2010,"Shetland","All major congenital conditions registerable by EUROCAT",9,"",260,346.2,""],
    [2256,2010,"Shetland","Nervous system conditions",0,"",260,0,""],
    [2257,2010,"Shetland","Eye conditions",0,"",260,0,""],
    [2260,2010,"Shetland","Respiratory conditions",0,"",260,0,""],
    [2264,2010,"Shetland","Kidney and urinary tract conditions",0,"",260,0,""],
    [2266,2010,"Shetland","Limb conditions",0,"",260,0,""],
    [2269,2010,"Tayside","All major congenital conditions registerable by EUROCAT",108,"",4315,250.3,""],
    [2270,2010,"Tayside","Nervous system conditions",8,"",4315,18.5,""],
    [2272,2010,"Tayside","Ear, face and neck conditions",0,"",4315,0,""],
    [2273,2010,"Tayside","Congenital heart diseases (CHD)",15,"",4315,34.8,""],
    [2274,2010,"Tayside","Respiratory conditions",0,"",4315,0,""],
    [2275,2010,"Tayside","Oro-facial clefts",6,"",4315,13.9,""],
    [2276,2010,"Tayside","Gastro-intestinal conditions",10,"",4315,23.2,""],
    [2279,2010,"Tayside","Genital conditions",22,"",4315,51,""],
    [2280,2010,"Tayside","Limb conditions",22,"",4315,51,""],
    [2282,2010,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",14,"",4315,32.4,""],
    [2283,2010,"Total","All major congenital conditions registerable by EUROCAT",1835,"",59133,310.3,""],
    [2284,2010,"Total","Nervous system conditions",162,"",59133,27.4,""],
    [2285,2010,"Total","Eye conditions",39,"",59133,6.6,""],
    [2286,2010,"Total","Ear, face and neck conditions",13,"",59133,2.2,""],
    [2287,2010,"Total","Congenital heart diseases (CHD)",431,"",59133,72.9,""],
    [2288,2010,"Total","Respiratory conditions",43,"",59133,7.3,""],
    [2289,2010,"Total","Oro-facial clefts",103,"",59133,17.4,""],
    [2290,2010,"Total","Gastro-intestinal conditions",154,"",59133,26,""],
    [2291,2010,"Total","Abdominal wall defects",41,"",59133,6.9,""],
    [2292,2010,"Total","Kidney and urinary tract conditions",156,"",59133,26.4,""],
    [2293,2010,"Total","Genital conditions",215,"",59133,36.4,""],
    [2294,2010,"Total","Limb conditions",302,"",59133,51.1,""],
    [2295,2010,"Total","Other conditions/syndromes",76,"",59133,12.9,""],
    [2296,2010,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",286,"",59133,48.4,""],
    [2297,2010,"Western Isles","All major congenital conditions registerable by EUROCAT",6,"",237,253.2,""],
    [2299,2010,"Western Isles","Eye conditions",0,"",237,0,""],
    [2300,2010,"Western Isles","Ear, face and neck conditions",0,"",237,0,""],
    [2301,2010,"Western Isles","Congenital heart diseases (CHD)",0,"",237,0,""],
    [2302,2010,"Western Isles","Respiratory conditions",0,"",237,0,""],
    [2303,2010,"Western Isles","Oro-facial clefts",0,"",237,0,""],
    [2305,2010,"Western Isles","Abdominal wall defects",0,"",237,0,""],
    [2307,2010,"Western Isles","Genital conditions",0,"",237,0,""],
    [2309,2010,"Western Isles","Other conditions/syndromes",0,"",237,0,""],
    [2310,2010,"Western Isles","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",237,0,""],
    [2311,2009,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",137,"",3896,351.6,""],
    [2312,2009,"Ayrshire and Arran","Nervous system conditions",14,"",3896,35.9,""],
    [2315,2009,"Ayrshire and Arran","Congenital heart diseases (CHD)",31,"",3896,79.6,""],
    [2317,2009,"Ayrshire and Arran","Oro-facial clefts",6,"",3896,15.4,""],
    [2318,2009,"Ayrshire and Arran","Gastro-intestinal conditions",16,"",3896,41.1,""],
    [2320,2009,"Ayrshire and Arran","Kidney and urinary tract conditions",17,"",3896,43.6,""],
    [2321,2009,"Ayrshire and Arran","Genital conditions",20,"",3896,51.3,""],
    [2322,2009,"Ayrshire and Arran","Limb conditions",22,"",3896,56.5,""],
    [2324,2009,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",21,"",3896,53.9,""],
    [2325,2009,"Borders","All major congenital conditions registerable by EUROCAT",20,"",1087,184,""],
    [2327,2009,"Borders","Eye conditions",0,"",1087,0,""],
    [2328,2009,"Borders","Ear, face and neck conditions",0,"",1087,0,""],
    [2329,2009,"Borders","Congenital heart diseases (CHD)",6,"",1087,55.2,""],
    [2338,2009,"Borders","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",5,"",1087,46,""],
    [2339,2009,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",47,"",1498,313.8,""],
    [2340,2009,"Dumfries and Galloway","Nervous system conditions",7,"",1498,46.7,""],
    [2341,2009,"Dumfries and Galloway","Eye conditions",0,"",1498,0,""],
    [2342,2009,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1498,0,""],
    [2343,2009,"Dumfries and Galloway","Congenital heart diseases (CHD)",6,"",1498,40.1,""],
    [2344,2009,"Dumfries and Galloway","Respiratory conditions",0,"",1498,0,""],
    [2348,2009,"Dumfries and Galloway","Kidney and urinary tract conditions",5,"",1498,33.4,""],
    [2350,2009,"Dumfries and Galloway","Limb conditions",10,"",1498,66.8,""],
    [2351,2009,"Dumfries and Galloway","Other conditions/syndromes",6,"",1498,40.1,""],
    [2352,2009,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",6,"",1498,40.1,""],
    [2353,2009,"Fife","All major congenital conditions registerable by EUROCAT",115,"",4234,271.6,""],
    [2354,2009,"Fife","Nervous system conditions",20,"",4234,47.2,""],
    [2356,2009,"Fife","Ear, face and neck conditions",0,"",4234,0,""],
    [2357,2009,"Fife","Congenital heart diseases (CHD)",40,"",4234,94.5,""],
    [2359,2009,"Fife","Oro-facial clefts",6,"",4234,14.2,""],
    [2360,2009,"Fife","Gastro-intestinal conditions",11,"",4234,26,""],
    [2362,2009,"Fife","Kidney and urinary tract conditions",6,"",4234,14.2,""],
    [2363,2009,"Fife","Genital conditions",9,"",4234,21.3,""],
    [2364,2009,"Fife","Limb conditions",7,"",4234,16.5,""],
    [2365,2009,"Fife","Other conditions/syndromes",7,"",4234,16.5,""],
    [2366,2009,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",24,"",4234,56.7,""],
    [2367,2009,"Forth Valley","All major congenital conditions registerable by EUROCAT",71,"",3379,210.1,""],
    [2368,2009,"Forth Valley","Nervous system conditions",6,"",3379,17.8,""],
    [2370,2009,"Forth Valley","Ear, face and neck conditions",0,"",3379,0,""],
    [2371,2009,"Forth Valley","Congenital heart diseases (CHD)",22,"",3379,65.1,""],
    [2373,2009,"Forth Valley","Oro-facial clefts",7,"",3379,20.7,""],
    [2374,2009,"Forth Valley","Gastro-intestinal conditions",6,"",3379,17.8,""],
    [2377,2009,"Forth Valley","Genital conditions",14,"",3379,41.4,""],
    [2380,2009,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",3379,44.4,""],
    [2381,2009,"Grampian","All major congenital conditions registerable by EUROCAT",278,"",6491,428.3,""],
    [2382,2009,"Grampian","Nervous system conditions",13,"",6491,20,""],
    [2385,2009,"Grampian","Congenital heart diseases (CHD)",58,"",6491,89.4,""],
    [2386,2009,"Grampian","Respiratory conditions",12,"",6491,18.5,""],
    [2387,2009,"Grampian","Oro-facial clefts",10,"",6491,15.4,""],
    [2388,2009,"Grampian","Gastro-intestinal conditions",15,"",6491,23.1,""],
    [2389,2009,"Grampian","Abdominal wall defects",5,"",6491,7.7,""],
    [2390,2009,"Grampian","Kidney and urinary tract conditions",25,"",6491,38.5,""],
    [2391,2009,"Grampian","Genital conditions",49,"",6491,75.5,""],
    [2392,2009,"Grampian","Limb conditions",67,"",6491,103.2,""],
    [2393,2009,"Grampian","Other conditions/syndromes",5,"",6491,7.7,""],
    [2394,2009,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",44,"",6491,67.8,""],
    [2395,2009,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",381,"",13090,291.1,""],
    [2396,2009,"Greater Glasgow and Clyde","Nervous system conditions",27,"",13090,20.6,""],
    [2397,2009,"Greater Glasgow and Clyde","Eye conditions",14,"",13090,10.7,""],
    [2398,2009,"Greater Glasgow and Clyde","Ear, face and neck conditions",0,"",13090,0,""],
    [2399,2009,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",79,"",13090,60.4,""],
    [2400,2009,"Greater Glasgow and Clyde","Respiratory conditions",13,"",13090,9.9,""],
    [2401,2009,"Greater Glasgow and Clyde","Oro-facial clefts",26,"",13090,19.9,""],
    [2402,2009,"Greater Glasgow and Clyde","Gastro-intestinal conditions",41,"",13090,31.3,""],
    [2403,2009,"Greater Glasgow and Clyde","Abdominal wall defects",6,"",13090,4.6,""],
    [2404,2009,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",30,"",13090,22.9,""],
    [2405,2009,"Greater Glasgow and Clyde","Genital conditions",45,"",13090,34.4,""],
    [2406,2009,"Greater Glasgow and Clyde","Limb conditions",67,"",13090,51.2,""],
    [2407,2009,"Greater Glasgow and Clyde","Other conditions/syndromes",22,"",13090,16.8,""],
    [2408,2009,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",44,"",13090,33.6,""],
    [2409,2009,"Highland","All major congenital conditions registerable by EUROCAT",133,"",3209,414.5,""],
    [2410,2009,"Highland","Nervous system conditions",12,"",3209,37.4,""],
    [2412,2009,"Highland","Ear, face and neck conditions",0,"",3209,0,""],
    [2413,2009,"Highland","Congenital heart diseases (CHD)",60,"",3209,187,""],
    [2415,2009,"Highland","Oro-facial clefts",6,"",3209,18.7,""],
    [2416,2009,"Highland","Gastro-intestinal conditions",5,"",3209,15.6,""],
    [2418,2009,"Highland","Kidney and urinary tract conditions",9,"",3209,28,""],
    [2419,2009,"Highland","Genital conditions",19,"",3209,59.2,""],
    [2420,2009,"Highland","Limb conditions",13,"",3209,40.5,""],
    [2422,2009,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",17,"",3209,53,""],
    [2423,2009,"Lanarkshire","All major congenital conditions registerable by EUROCAT",196,"",7620,257.2,""],
    [2424,2009,"Lanarkshire","Nervous system conditions",17,"",7620,22.3,""],
    [2425,2009,"Lanarkshire","Eye conditions",0,"",7620,0,""],
    [2426,2009,"Lanarkshire","Ear, face and neck conditions",0,"",7620,0,""],
    [2427,2009,"Lanarkshire","Congenital heart diseases (CHD)",42,"",7620,55.1,""],
    [2428,2009,"Lanarkshire","Respiratory conditions",7,"",7620,9.2,""],
    [2429,2009,"Lanarkshire","Oro-facial clefts",10,"",7620,13.1,""],
    [2430,2009,"Lanarkshire","Gastro-intestinal conditions",18,"",7620,23.6,""],
    [2431,2009,"Lanarkshire","Abdominal wall defects",9,"",7620,11.8,""],
    [2432,2009,"Lanarkshire","Kidney and urinary tract conditions",8,"",7620,10.5,""],
    [2433,2009,"Lanarkshire","Genital conditions",18,"",7620,23.6,""],
    [2434,2009,"Lanarkshire","Limb conditions",32,"",7620,42,""],
    [2435,2009,"Lanarkshire","Other conditions/syndromes",14,"",7620,18.4,""],
    [2436,2009,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",33,"",7620,43.3,""],
    [2437,2009,"Lothian","All major congenital conditions registerable by EUROCAT",373,"",9741,382.9,""],
    [2438,2009,"Lothian","Nervous system conditions",32,"",9741,32.9,""],
    [2439,2009,"Lothian","Eye conditions",8,"",9741,8.2,""],
    [2440,2009,"Lothian","Ear, face and neck conditions",7,"",9741,7.2,""],
    [2441,2009,"Lothian","Congenital heart diseases (CHD)",54,"",9741,55.4,""],
    [2443,2009,"Lothian","Oro-facial clefts",16,"",9741,16.4,""],
    [2444,2009,"Lothian","Gastro-intestinal conditions",25,"",9741,25.7,""],
    [2445,2009,"Lothian","Abdominal wall defects",9,"",9741,9.2,""],
    [2446,2009,"Lothian","Kidney and urinary tract conditions",20,"",9741,20.5,""],
    [2447,2009,"Lothian","Genital conditions",52,"",9741,53.4,""],
    [2448,2009,"Lothian","Limb conditions",97,"",9741,99.6,""],
    [2449,2009,"Lothian","Other conditions/syndromes",19,"",9741,19.5,""],
    [2450,2009,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",63,"",9741,64.7,""],
    [2452,2009,"Orkney","Nervous system conditions",0,"",198,0,""],
    [2453,2009,"Orkney","Eye conditions",0,"",198,0,""],
    [2454,2009,"Orkney","Ear, face and neck conditions",0,"",198,0,""],
    [2456,2009,"Orkney","Respiratory conditions",0,"",198,0,""],
    [2457,2009,"Orkney","Oro-facial clefts",0,"",198,0,""],
    [2458,2009,"Orkney","Gastro-intestinal conditions",0,"",198,0,""],
    [2459,2009,"Orkney","Abdominal wall defects",0,"",198,0,""],
    [2461,2009,"Orkney","Genital conditions",0,"",198,0,""],
    [2462,2009,"Orkney","Limb conditions",0,"",198,0,""],
    [2463,2009,"Orkney","Other conditions/syndromes",0,"",198,0,""],
    [2467,2009,"Shetland","Eye conditions",0,"",286,0,""],
    [2468,2009,"Shetland","Ear, face and neck conditions",0,"",286,0,""],
    [2470,2009,"Shetland","Respiratory conditions",0,"",286,0,""],
    [2471,2009,"Shetland","Oro-facial clefts",0,"",286,0,""],
    [2472,2009,"Shetland","Gastro-intestinal conditions",0,"",286,0,""],
    [2473,2009,"Shetland","Abdominal wall defects",0,"",286,0,""],
    [2474,2009,"Shetland","Kidney and urinary tract conditions",0,"",286,0,""],
    [2475,2009,"Shetland","Genital conditions",0,"",286,0,""],
    [2479,2009,"Tayside","All major congenital conditions registerable by EUROCAT",155,"",4380,353.9,""],
    [2480,2009,"Tayside","Nervous system conditions",18,"",4380,41.1,""],
    [2482,2009,"Tayside","Ear, face and neck conditions",0,"",4380,0,""],
    [2483,2009,"Tayside","Congenital heart diseases (CHD)",27,"",4380,61.6,""],
    [2485,2009,"Tayside","Oro-facial clefts",6,"",4380,13.7,""],
    [2486,2009,"Tayside","Gastro-intestinal conditions",18,"",4380,41.1,""],
    [2487,2009,"Tayside","Abdominal wall defects",9,"",4380,20.5,""],
    [2488,2009,"Tayside","Kidney and urinary tract conditions",15,"",4380,34.2,""],
    [2489,2009,"Tayside","Genital conditions",24,"",4380,54.8,""],
    [2490,2009,"Tayside","Limb conditions",22,"",4380,50.2,""],
    [2491,2009,"Tayside","Other conditions/syndromes",7,"",4380,16,""],
    [2492,2009,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",24,"",4380,54.8,""],
    [2493,2009,"Total","All major congenital conditions registerable by EUROCAT",1920,"",59528,322.5,""],
    [2494,2009,"Total","Nervous system conditions",173,"",59528,29.1,""],
    [2495,2009,"Total","Eye conditions",37,"",59528,6.2,""],
    [2496,2009,"Total","Ear, face and neck conditions",12,"",59528,2,""],
    [2497,2009,"Total","Congenital heart diseases (CHD)",431,"",59528,72.4,""],
    [2498,2009,"Total","Respiratory conditions",48,"",59528,8.1,""],
    [2499,2009,"Total","Oro-facial clefts",97,"",59528,16.3,""],
    [2500,2009,"Total","Gastro-intestinal conditions",162,"",59528,27.2,""],
    [2501,2009,"Total","Abdominal wall defects",53,"",59528,8.9,""],
    [2502,2009,"Total","Kidney and urinary tract conditions",139,"",59528,23.4,""],
    [2503,2009,"Total","Genital conditions",256,"",59528,43,""],
    [2504,2009,"Total","Limb conditions",343,"",59528,57.6,""],
    [2505,2009,"Total","Other conditions/syndromes",94,"",59528,15.8,""],
    [2506,2009,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",300,"",59528,50.4,""],
    [2509,2009,"Western Isles","Eye conditions",0,"",216,0,""],
    [2510,2009,"Western Isles","Ear, face and neck conditions",0,"",216,0,""],
    [2512,2009,"Western Isles","Respiratory conditions",0,"",216,0,""],
    [2513,2009,"Western Isles","Oro-facial clefts",0,"",216,0,""],
    [2514,2009,"Western Isles","Gastro-intestinal conditions",0,"",216,0,""],
    [2515,2009,"Western Isles","Abdominal wall defects",0,"",216,0,""],
    [2516,2009,"Western Isles","Kidney and urinary tract conditions",0,"",216,0,""],
    [2518,2009,"Western Isles","Limb conditions",0,"",216,0,""],
    [2519,2009,"Western Isles","Other conditions/syndromes",0,"",216,0,""],
    [2521,2008,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",110,"",3909,281.4,""],
    [2522,2008,"Ayrshire and Arran","Nervous system conditions",9,"",3909,23,""],
    [2523,2008,"Ayrshire and Arran","Eye conditions",5,"",3909,12.8,""],
    [2524,2008,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3909,0,""],
    [2525,2008,"Ayrshire and Arran","Congenital heart diseases (CHD)",32,"",3909,81.9,""],
    [2527,2008,"Ayrshire and Arran","Oro-facial clefts",5,"",3909,12.8,""],
    [2528,2008,"Ayrshire and Arran","Gastro-intestinal conditions",9,"",3909,23,""],
    [2530,2008,"Ayrshire and Arran","Kidney and urinary tract conditions",7,"",3909,17.9,""],
    [2531,2008,"Ayrshire and Arran","Genital conditions",10,"",3909,25.6,""],
    [2532,2008,"Ayrshire and Arran","Limb conditions",25,"",3909,64,""],
    [2534,2008,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",3909,40.9,""],
    [2535,2008,"Borders","All major congenital conditions registerable by EUROCAT",26,"",1087,239.2,""],
    [2536,2008,"Borders","Nervous system conditions",5,"",1087,46,""],
    [2537,2008,"Borders","Eye conditions",0,"",1087,0,""],
    [2538,2008,"Borders","Ear, face and neck conditions",0,"",1087,0,""],
    [2539,2008,"Borders","Congenital heart diseases (CHD)",8,"",1087,73.6,""],
    [2541,2008,"Borders","Oro-facial clefts",6,"",1087,55.2,""],
    [2544,2008,"Borders","Kidney and urinary tract conditions",0,"",1087,0,""],
    [2545,2008,"Borders","Genital conditions",0,"",1087,0,""],
    [2548,2008,"Borders","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",5,"",1087,46,""],
    [2549,2008,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",59,"",1434,411.4,""],
    [2550,2008,"Dumfries and Galloway","Nervous system conditions",8,"",1434,55.8,""],
    [2552,2008,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1434,0,""],
    [2553,2008,"Dumfries and Galloway","Congenital heart diseases (CHD)",10,"",1434,69.7,""],
    [2556,2008,"Dumfries and Galloway","Gastro-intestinal conditions",8,"",1434,55.8,""],
    [2558,2008,"Dumfries and Galloway","Kidney and urinary tract conditions",12,"",1434,83.7,""],
    [2560,2008,"Dumfries and Galloway","Limb conditions",11,"",1434,76.7,""],
    [2561,2008,"Dumfries and Galloway","Other conditions/syndromes",0,"",1434,0,""],
    [2562,2008,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",10,"",1434,69.7,""],
    [2563,2008,"Fife","All major congenital conditions registerable by EUROCAT",109,"",4306,253.1,""],
    [2564,2008,"Fife","Nervous system conditions",15,"",4306,34.8,""],
    [2565,2008,"Fife","Eye conditions",5,"",4306,11.6,""],
    [2567,2008,"Fife","Congenital heart diseases (CHD)",18,"",4306,41.8,""],
    [2569,2008,"Fife","Oro-facial clefts",7,"",4306,16.3,""],
    [2570,2008,"Fife","Gastro-intestinal conditions",8,"",4306,18.6,""],
    [2571,2008,"Fife","Abdominal wall defects",6,"",4306,13.9,""],
    [2572,2008,"Fife","Kidney and urinary tract conditions",9,"",4306,20.9,""],
    [2573,2008,"Fife","Genital conditions",10,"",4306,23.2,""],
    [2574,2008,"Fife","Limb conditions",11,"",4306,25.5,""],
    [2575,2008,"Fife","Other conditions/syndromes",6,"",4306,13.9,""],
    [2576,2008,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",27,"",4306,62.7,""],
    [2577,2008,"Forth Valley","All major congenital conditions registerable by EUROCAT",86,"",3454,249,""],
    [2578,2008,"Forth Valley","Nervous system conditions",12,"",3454,34.7,""],
    [2581,2008,"Forth Valley","Congenital heart diseases (CHD)",16,"",3454,46.3,""],
    [2583,2008,"Forth Valley","Oro-facial clefts",7,"",3454,20.3,""],
    [2584,2008,"Forth Valley","Gastro-intestinal conditions",11,"",3454,31.8,""],
    [2585,2008,"Forth Valley","Abdominal wall defects",6,"",3454,17.4,""],
    [2587,2008,"Forth Valley","Genital conditions",11,"",3454,31.8,""],
    [2588,2008,"Forth Valley","Limb conditions",5,"",3454,14.5,""],
    [2589,2008,"Forth Valley","Other conditions/syndromes",7,"",3454,20.3,""],
    [2590,2008,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",11,"",3454,31.8,""],
    [2591,2008,"Grampian","All major congenital conditions registerable by EUROCAT",281,"",6338,443.4,""],
    [2592,2008,"Grampian","Nervous system conditions",25,"",6338,39.4,""],
    [2595,2008,"Grampian","Congenital heart diseases (CHD)",66,"",6338,104.1,""],
    [2597,2008,"Grampian","Oro-facial clefts",17,"",6338,26.8,""],
    [2598,2008,"Grampian","Gastro-intestinal conditions",15,"",6338,23.7,""],
    [2600,2008,"Grampian","Kidney and urinary tract conditions",26,"",6338,41,""],
    [2601,2008,"Grampian","Genital conditions",32,"",6338,50.5,""],
    [2602,2008,"Grampian","Limb conditions",56,"",6338,88.4,""],
    [2603,2008,"Grampian","Other conditions/syndromes",12,"",6338,18.9,""],
    [2604,2008,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",44,"",6338,69.4,""],
    [2605,2008,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",368,"",13108,280.7,""],
    [2606,2008,"Greater Glasgow and Clyde","Nervous system conditions",33,"",13108,25.2,""],
    [2609,2008,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",70,"",13108,53.4,""],
    [2610,2008,"Greater Glasgow and Clyde","Respiratory conditions",16,"",13108,12.2,""],
    [2611,2008,"Greater Glasgow and Clyde","Oro-facial clefts",34,"",13108,25.9,""],
    [2612,2008,"Greater Glasgow and Clyde","Gastro-intestinal conditions",26,"",13108,19.8,""],
    [2613,2008,"Greater Glasgow and Clyde","Abdominal wall defects",9,"",13108,6.9,""],
    [2614,2008,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",34,"",13108,25.9,""],
    [2615,2008,"Greater Glasgow and Clyde","Genital conditions",46,"",13108,35.1,""],
    [2616,2008,"Greater Glasgow and Clyde","Limb conditions",53,"",13108,40.4,""],
    [2617,2008,"Greater Glasgow and Clyde","Other conditions/syndromes",15,"",13108,11.4,""],
    [2618,2008,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",52,"",13108,39.7,""],
    [2619,2008,"Highland","All major congenital conditions registerable by EUROCAT",103,"",3303,311.8,""],
    [2620,2008,"Highland","Nervous system conditions",10,"",3303,30.3,""],
    [2622,2008,"Highland","Ear, face and neck conditions",0,"",3303,0,""],
    [2623,2008,"Highland","Congenital heart diseases (CHD)",37,"",3303,112,""],
    [2625,2008,"Highland","Oro-facial clefts",5,"",3303,15.1,""],
    [2626,2008,"Highland","Gastro-intestinal conditions",7,"",3303,21.2,""],
    [2628,2008,"Highland","Kidney and urinary tract conditions",9,"",3303,27.2,""],
    [2629,2008,"Highland","Genital conditions",10,"",3303,30.3,""],
    [2630,2008,"Highland","Limb conditions",9,"",3303,27.2,""],
    [2632,2008,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",13,"",3303,39.4,""],
    [2633,2008,"Lanarkshire","All major congenital conditions registerable by EUROCAT",167,"",7861,212.4,""],
    [2634,2008,"Lanarkshire","Nervous system conditions",12,"",7861,15.3,""],
    [2637,2008,"Lanarkshire","Congenital heart diseases (CHD)",43,"",7861,54.7,""],
    [2638,2008,"Lanarkshire","Respiratory conditions",8,"",7861,10.2,""],
    [2639,2008,"Lanarkshire","Oro-facial clefts",8,"",7861,10.2,""],
    [2640,2008,"Lanarkshire","Gastro-intestinal conditions",16,"",7861,20.4,""],
    [2642,2008,"Lanarkshire","Kidney and urinary tract conditions",13,"",7861,16.5,""],
    [2643,2008,"Lanarkshire","Genital conditions",26,"",7861,33.1,""],
    [2644,2008,"Lanarkshire","Limb conditions",19,"",7861,24.2,""],
    [2645,2008,"Lanarkshire","Other conditions/syndromes",7,"",7861,8.9,""],
    [2646,2008,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",23,"",7861,29.3,""],
    [2647,2008,"Lothian","All major congenital conditions registerable by EUROCAT",345,"",9850,350.3,""],
    [2648,2008,"Lothian","Nervous system conditions",22,"",9850,22.3,""],
    [2649,2008,"Lothian","Eye conditions",7,"",9850,7.1,""],
    [2650,2008,"Lothian","Ear, face and neck conditions",9,"",9850,9.1,""],
    [2651,2008,"Lothian","Congenital heart diseases (CHD)",47,"",9850,47.7,""],
    [2652,2008,"Lothian","Respiratory conditions",6,"",9850,6.1,""],
    [2653,2008,"Lothian","Oro-facial clefts",18,"",9850,18.3,""],
    [2654,2008,"Lothian","Gastro-intestinal conditions",42,"",9850,42.6,""],
    [2655,2008,"Lothian","Abdominal wall defects",7,"",9850,7.1,""],
    [2656,2008,"Lothian","Kidney and urinary tract conditions",13,"",9850,13.2,""],
    [2657,2008,"Lothian","Genital conditions",53,"",9850,53.8,""],
    [2658,2008,"Lothian","Limb conditions",66,"",9850,67,""],
    [2659,2008,"Lothian","Other conditions/syndromes",13,"",9850,13.2,""],
    [2660,2008,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",70,"",9850,71.1,""],
    [2662,2008,"Orkney","Nervous system conditions",0,"",218,0,""],
    [2663,2008,"Orkney","Eye conditions",0,"",218,0,""],
    [2664,2008,"Orkney","Ear, face and neck conditions",0,"",218,0,""],
    [2667,2008,"Orkney","Oro-facial clefts",0,"",218,0,""],
    [2669,2008,"Orkney","Abdominal wall defects",0,"",218,0,""],
    [2670,2008,"Orkney","Kidney and urinary tract conditions",0,"",218,0,""],
    [2671,2008,"Orkney","Genital conditions",0,"",218,0,""],
    [2673,2008,"Orkney","Other conditions/syndromes",0,"",218,0,""],
    [2674,2008,"Orkney","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",218,0,""],
    [2675,2008,"Shetland","All major congenital conditions registerable by EUROCAT",8,"",268,298.5,""],
    [2676,2008,"Shetland","Nervous system conditions",0,"",268,0,""],
    [2677,2008,"Shetland","Eye conditions",0,"",268,0,""],
    [2678,2008,"Shetland","Ear, face and neck conditions",0,"",268,0,""],
    [2680,2008,"Shetland","Respiratory conditions",0,"",268,0,""],
    [2681,2008,"Shetland","Oro-facial clefts",0,"",268,0,""],
    [2683,2008,"Shetland","Abdominal wall defects",0,"",268,0,""],
    [2684,2008,"Shetland","Kidney and urinary tract conditions",0,"",268,0,""],
    [2685,2008,"Shetland","Genital conditions",0,"",268,0,""],
    [2687,2008,"Shetland","Other conditions/syndromes",0,"",268,0,""],
    [2689,2008,"Tayside","All major congenital conditions registerable by EUROCAT",111,"",4420,251.1,""],
    [2690,2008,"Tayside","Nervous system conditions",5,"",4420,11.3,""],
    [2692,2008,"Tayside","Ear, face and neck conditions",0,"",4420,0,""],
    [2693,2008,"Tayside","Congenital heart diseases (CHD)",16,"",4420,36.2,""],
    [2695,2008,"Tayside","Oro-facial clefts",10,"",4420,22.6,""],
    [2696,2008,"Tayside","Gastro-intestinal conditions",8,"",4420,18.1,""],
    [2697,2008,"Tayside","Abdominal wall defects",6,"",4420,13.6,""],
    [2698,2008,"Tayside","Kidney and urinary tract conditions",10,"",4420,22.6,""],
    [2699,2008,"Tayside","Genital conditions",17,"",4420,38.5,""],
    [2700,2008,"Tayside","Limb conditions",16,"",4420,36.2,""],
    [2701,2008,"Tayside","Other conditions/syndromes",10,"",4420,22.6,""],
    [2702,2008,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",23,"",4420,52,""],
    [2703,2008,"Total","All major congenital conditions registerable by EUROCAT",1785,"",60052,297.2,""],
    [2704,2008,"Total","Nervous system conditions",156,"",60052,26,""],
    [2705,2008,"Total","Eye conditions",33,"",60052,5.5,""],
    [2706,2008,"Total","Ear, face and neck conditions",18,"",60052,3,""],
    [2707,2008,"Total","Congenital heart diseases (CHD)",371,"",60052,61.8,""],
    [2708,2008,"Total","Respiratory conditions",51,"",60052,8.5,""],
    [2709,2008,"Total","Oro-facial clefts",120,"",60052,20,""],
    [2710,2008,"Total","Gastro-intestinal conditions",159,"",60052,26.5,""],
    [2711,2008,"Total","Abdominal wall defects",47,"",60052,7.8,""],
    [2712,2008,"Total","Kidney and urinary tract conditions",137,"",60052,22.8,""],
    [2713,2008,"Total","Genital conditions",217,"",60052,36.1,""],
    [2714,2008,"Total","Limb conditions",278,"",60052,46.3,""],
    [2715,2008,"Total","Other conditions/syndromes",77,"",60052,12.8,""],
    [2716,2008,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",298,"",60052,49.6,""],
    [2717,2008,"Western Isles","All major congenital conditions registerable by EUROCAT",6,"",262,229,""],
    [2718,2008,"Western Isles","Nervous system conditions",0,"",262,0,""],
    [2719,2008,"Western Isles","Eye conditions",0,"",262,0,""],
    [2720,2008,"Western Isles","Ear, face and neck conditions",0,"",262,0,""],
    [2722,2008,"Western Isles","Respiratory conditions",0,"",262,0,""],
    [2725,2008,"Western Isles","Abdominal wall defects",0,"",262,0,""],
    [2726,2008,"Western Isles","Kidney and urinary tract conditions",0,"",262,0,""],
    [2727,2008,"Western Isles","Genital conditions",0,"",262,0,""],
    [2729,2008,"Western Isles","Other conditions/syndromes",0,"",262,0,""],
    [2731,2007,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",142,"",3878,366.2,""],
    [2732,2007,"Ayrshire and Arran","Nervous system conditions",24,"",3878,61.9,""],
    [2733,2007,"Ayrshire and Arran","Eye conditions",5,"",3878,12.9,""],
    [2735,2007,"Ayrshire and Arran","Congenital heart diseases (CHD)",31,"",3878,79.9,""],
    [2736,2007,"Ayrshire and Arran","Respiratory conditions",0,"",3878,0,""],
    [2737,2007,"Ayrshire and Arran","Oro-facial clefts",7,"",3878,18.1,""],
    [2738,2007,"Ayrshire and Arran","Gastro-intestinal conditions",13,"",3878,33.5,""],
    [2740,2007,"Ayrshire and Arran","Kidney and urinary tract conditions",16,"",3878,41.3,""],
    [2741,2007,"Ayrshire and Arran","Genital conditions",15,"",3878,38.7,""],
    [2742,2007,"Ayrshire and Arran","Limb conditions",14,"",3878,36.1,""],
    [2743,2007,"Ayrshire and Arran","Other conditions/syndromes",9,"",3878,23.2,""],
    [2744,2007,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",28,"",3878,72.2,""],
    [2745,2007,"Borders","All major congenital conditions registerable by EUROCAT",12,"",1109,108.2,""],
    [2747,2007,"Borders","Eye conditions",0,"",1109,0,""],
    [2748,2007,"Borders","Ear, face and neck conditions",0,"",1109,0,""],
    [2750,2007,"Borders","Respiratory conditions",0,"",1109,0,""],
    [2754,2007,"Borders","Kidney and urinary tract conditions",0,"",1109,0,""],
    [2755,2007,"Borders","Genital conditions",0,"",1109,0,""],
    [2759,2007,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",56,"",1464,382.5,""],
    [2760,2007,"Dumfries and Galloway","Nervous system conditions",7,"",1464,47.8,""],
    [2762,2007,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1464,0,""],
    [2763,2007,"Dumfries and Galloway","Congenital heart diseases (CHD)",7,"",1464,47.8,""],
    [2764,2007,"Dumfries and Galloway","Respiratory conditions",0,"",1464,0,""],
    [2765,2007,"Dumfries and Galloway","Oro-facial clefts",5,"",1464,34.2,""],
    [2766,2007,"Dumfries and Galloway","Gastro-intestinal conditions",7,"",1464,47.8,""],
    [2767,2007,"Dumfries and Galloway","Abdominal wall defects",0,"",1464,0,""],
    [2768,2007,"Dumfries and Galloway","Kidney and urinary tract conditions",11,"",1464,75.1,""],
    [2769,2007,"Dumfries and Galloway","Genital conditions",6,"",1464,41,""],
    [2770,2007,"Dumfries and Galloway","Limb conditions",6,"",1464,41,""],
    [2772,2007,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",9,"",1464,61.5,""],
    [2773,2007,"Fife","All major congenital conditions registerable by EUROCAT",100,"",4132,242,""],
    [2774,2007,"Fife","Nervous system conditions",10,"",4132,24.2,""],
    [2777,2007,"Fife","Congenital heart diseases (CHD)",31,"",4132,75,""],
    [2779,2007,"Fife","Oro-facial clefts",5,"",4132,12.1,""],
    [2780,2007,"Fife","Gastro-intestinal conditions",8,"",4132,19.4,""],
    [2781,2007,"Fife","Abdominal wall defects",5,"",4132,12.1,""],
    [2782,2007,"Fife","Kidney and urinary tract conditions",10,"",4132,24.2,""],
    [2783,2007,"Fife","Genital conditions",8,"",4132,19.4,""],
    [2784,2007,"Fife","Limb conditions",11,"",4132,26.6,""],
    [2785,2007,"Fife","Other conditions/syndromes",9,"",4132,21.8,""],
    [2786,2007,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",22,"",4132,53.2,""],
    [2787,2007,"Forth Valley","All major congenital conditions registerable by EUROCAT",88,"",3425,256.9,""],
    [2788,2007,"Forth Valley","Nervous system conditions",14,"",3425,40.9,""],
    [2790,2007,"Forth Valley","Ear, face and neck conditions",0,"",3425,0,""],
    [2791,2007,"Forth Valley","Congenital heart diseases (CHD)",15,"",3425,43.8,""],
    [2793,2007,"Forth Valley","Oro-facial clefts",12,"",3425,35,""],
    [2794,2007,"Forth Valley","Gastro-intestinal conditions",9,"",3425,26.3,""],
    [2795,2007,"Forth Valley","Abdominal wall defects",5,"",3425,14.6,""],
    [2796,2007,"Forth Valley","Kidney and urinary tract conditions",9,"",3425,26.3,""],
    [2797,2007,"Forth Valley","Genital conditions",12,"",3425,35,""],
    [2798,2007,"Forth Valley","Limb conditions",7,"",3425,20.4,""],
    [2799,2007,"Forth Valley","Other conditions/syndromes",6,"",3425,17.5,""],
    [2800,2007,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",12,"",3425,35,""],
    [2801,2007,"Grampian","All major congenital conditions registerable by EUROCAT",271,"",6091,444.9,""],
    [2802,2007,"Grampian","Nervous system conditions",21,"",6091,34.5,""],
    [2803,2007,"Grampian","Eye conditions",6,"",6091,9.9,""],
    [2805,2007,"Grampian","Congenital heart diseases (CHD)",72,"",6091,118.2,""],
    [2807,2007,"Grampian","Oro-facial clefts",7,"",6091,11.5,""],
    [2808,2007,"Grampian","Gastro-intestinal conditions",20,"",6091,32.8,""],
    [2810,2007,"Grampian","Kidney and urinary tract conditions",23,"",6091,37.8,""],
    [2811,2007,"Grampian","Genital conditions",27,"",6091,44.3,""],
    [2812,2007,"Grampian","Limb conditions",51,"",6091,83.7,""],
    [2813,2007,"Grampian","Other conditions/syndromes",10,"",6091,16.4,""],
    [2814,2007,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",52,"",6091,85.4,""],
    [2815,2007,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",350,"",12859,272.2,""],
    [2816,2007,"Greater Glasgow and Clyde","Nervous system conditions",27,"",12859,21,""],
    [2817,2007,"Greater Glasgow and Clyde","Eye conditions",7,"",12859,5.4,""],
    [2819,2007,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",59,"",12859,45.9,""],
    [2820,2007,"Greater Glasgow and Clyde","Respiratory conditions",17,"",12859,13.2,""],
    [2821,2007,"Greater Glasgow and Clyde","Oro-facial clefts",19,"",12859,14.8,""],
    [2822,2007,"Greater Glasgow and Clyde","Gastro-intestinal conditions",35,"",12859,27.2,""],
    [2823,2007,"Greater Glasgow and Clyde","Abdominal wall defects",9,"",12859,7,""],
    [2824,2007,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",40,"",12859,31.1,""],
    [2825,2007,"Greater Glasgow and Clyde","Genital conditions",52,"",12859,40.4,""],
    [2826,2007,"Greater Glasgow and Clyde","Limb conditions",37,"",12859,28.8,""],
    [2827,2007,"Greater Glasgow and Clyde","Other conditions/syndromes",21,"",12859,16.3,""],
    [2828,2007,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",35,"",12859,27.2,""],
    [2829,2007,"Highland","All major congenital conditions registerable by EUROCAT",104,"",3072,338.5,""],
    [2830,2007,"Highland","Nervous system conditions",10,"",3072,32.6,""],
    [2833,2007,"Highland","Congenital heart diseases (CHD)",41,"",3072,133.5,""],
    [2834,2007,"Highland","Respiratory conditions",0,"",3072,0,""],
    [2835,2007,"Highland","Oro-facial clefts",6,"",3072,19.5,""],
    [2838,2007,"Highland","Kidney and urinary tract conditions",8,"",3072,26,""],
    [2839,2007,"Highland","Genital conditions",10,"",3072,32.6,""],
    [2840,2007,"Highland","Limb conditions",11,"",3072,35.8,""],
    [2842,2007,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",17,"",3072,55.3,""],
    [2843,2007,"Lanarkshire","All major congenital conditions registerable by EUROCAT",177,"",7552,234.4,""],
    [2844,2007,"Lanarkshire","Nervous system conditions",21,"",7552,27.8,""],
    [2847,2007,"Lanarkshire","Congenital heart diseases (CHD)",44,"",7552,58.3,""],
    [2849,2007,"Lanarkshire","Oro-facial clefts",15,"",7552,19.9,""],
    [2850,2007,"Lanarkshire","Gastro-intestinal conditions",17,"",7552,22.5,""],
    [2851,2007,"Lanarkshire","Abdominal wall defects",5,"",7552,6.6,""],
    [2853,2007,"Lanarkshire","Genital conditions",28,"",7552,37.1,""],
    [2854,2007,"Lanarkshire","Limb conditions",27,"",7552,35.8,""],
    [2855,2007,"Lanarkshire","Other conditions/syndromes",6,"",7552,7.9,""],
    [2856,2007,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",21,"",7552,27.8,""],
    [2857,2007,"Lothian","All major congenital conditions registerable by EUROCAT",322,"",9501,338.9,""],
    [2858,2007,"Lothian","Nervous system conditions",20,"",9501,21.1,""],
    [2861,2007,"Lothian","Congenital heart diseases (CHD)",61,"",9501,64.2,""],
    [2863,2007,"Lothian","Oro-facial clefts",16,"",9501,16.8,""],
    [2864,2007,"Lothian","Gastro-intestinal conditions",28,"",9501,29.5,""],
    [2866,2007,"Lothian","Kidney and urinary tract conditions",18,"",9501,18.9,""],
    [2867,2007,"Lothian","Genital conditions",60,"",9501,63.2,""],
    [2868,2007,"Lothian","Limb conditions",77,"",9501,81,""],
    [2869,2007,"Lothian","Other conditions/syndromes",8,"",9501,8.4,""],
    [2870,2007,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",65,"",9501,68.4,""],
    [2871,2007,"Orkney","All major congenital conditions registerable by EUROCAT",5,"",191,261.8,""],
    [2873,2007,"Orkney","Eye conditions",0,"",191,0,""],
    [2874,2007,"Orkney","Ear, face and neck conditions",0,"",191,0,""],
    [2876,2007,"Orkney","Respiratory conditions",0,"",191,0,""],
    [2877,2007,"Orkney","Oro-facial clefts",0,"",191,0,""],
    [2878,2007,"Orkney","Gastro-intestinal conditions",0,"",191,0,""],
    [2879,2007,"Orkney","Abdominal wall defects",0,"",191,0,""],
    [2880,2007,"Orkney","Kidney and urinary tract conditions",0,"",191,0,""],
    [2881,2007,"Orkney","Genital conditions",0,"",191,0,""],
    [2882,2007,"Orkney","Limb conditions",0,"",191,0,""],
    [2883,2007,"Orkney","Other conditions/syndromes",0,"",191,0,""],
    [2884,2007,"Orkney","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",191,0,""],
    [2885,2007,"Shetland","All major congenital conditions registerable by EUROCAT",7,"",248,282.3,""],
    [2886,2007,"Shetland","Nervous system conditions",0,"",248,0,""],
    [2887,2007,"Shetland","Eye conditions",0,"",248,0,""],
    [2888,2007,"Shetland","Ear, face and neck conditions",0,"",248,0,""],
    [2889,2007,"Shetland","Congenital heart diseases (CHD)",5,"",248,201.6,""],
    [2890,2007,"Shetland","Respiratory conditions",0,"",248,0,""],
    [2891,2007,"Shetland","Oro-facial clefts",0,"",248,0,""],
    [2893,2007,"Shetland","Abdominal wall defects",0,"",248,0,""],
    [2897,2007,"Shetland","Other conditions/syndromes",0,"",248,0,""],
    [2899,2007,"Tayside","All major congenital conditions registerable by EUROCAT",97,"",4226,229.5,""],
    [2900,2007,"Tayside","Nervous system conditions",11,"",4226,26,""],
    [2903,2007,"Tayside","Congenital heart diseases (CHD)",17,"",4226,40.2,""],
    [2906,2007,"Tayside","Gastro-intestinal conditions",7,"",4226,16.6,""],
    [2908,2007,"Tayside","Kidney and urinary tract conditions",10,"",4226,23.7,""],
    [2909,2007,"Tayside","Genital conditions",14,"",4226,33.1,""],
    [2910,2007,"Tayside","Limb conditions",14,"",4226,33.1,""],
    [2912,2007,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",4226,35.5,""],
    [2913,2007,"Total","All major congenital conditions registerable by EUROCAT",1741,"",58222,299,""],
    [2914,2007,"Total","Nervous system conditions",170,"",58222,29.2,""],
    [2915,2007,"Total","Eye conditions",34,"",58222,5.8,""],
    [2916,2007,"Total","Ear, face and neck conditions",14,"",58222,2.4,""],
    [2917,2007,"Total","Congenital heart diseases (CHD)",390,"",58222,67,""],
    [2918,2007,"Total","Respiratory conditions",35,"",58222,6,""],
    [2919,2007,"Total","Oro-facial clefts",100,"",58222,17.2,""],
    [2920,2007,"Total","Gastro-intestinal conditions",154,"",58222,26.5,""],
    [2921,2007,"Total","Abdominal wall defects",40,"",58222,6.9,""],
    [2922,2007,"Total","Kidney and urinary tract conditions",152,"",58222,26.1,""],
    [2923,2007,"Total","Genital conditions",234,"",58222,40.2,""],
    [2924,2007,"Total","Limb conditions",260,"",58222,44.7,""],
    [2925,2007,"Total","Other conditions/syndromes",80,"",58222,13.7,""],
    [2926,2007,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",281,"",58222,48.3,""],
    [2927,2007,"Western Isles","All major congenital conditions registerable by EUROCAT",9,"",263,342.2,""],
    [2928,2007,"Western Isles","Nervous system conditions",0,"",263,0,""],
    [2930,2007,"Western Isles","Ear, face and neck conditions",0,"",263,0,""],
    [2932,2007,"Western Isles","Respiratory conditions",0,"",263,0,""],
    [2935,2007,"Western Isles","Abdominal wall defects",0,"",263,0,""],
    [2936,2007,"Western Isles","Kidney and urinary tract conditions",0,"",263,0,""],
    [2937,2007,"Western Isles","Genital conditions",0,"",263,0,""],
    [2938,2007,"Western Isles","Limb conditions",0,"",263,0,""],
    [2939,2007,"Western Isles","Other conditions/syndromes",0,"",263,0,""],
    [2941,2006,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",107,"",3857,277.4,""],
    [2942,2006,"Ayrshire and Arran","Nervous system conditions",18,"",3857,46.7,""],
    [2943,2006,"Ayrshire and Arran","Eye conditions",0,"",3857,0,""],
    [2944,2006,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3857,0,""],
    [2945,2006,"Ayrshire and Arran","Congenital heart diseases (CHD)",18,"",3857,46.7,""],
    [2947,2006,"Ayrshire and Arran","Oro-facial clefts",5,"",3857,13,""],
    [2948,2006,"Ayrshire and Arran","Gastro-intestinal conditions",8,"",3857,20.7,""],
    [2950,2006,"Ayrshire and Arran","Kidney and urinary tract conditions",14,"",3857,36.3,""],
    [2951,2006,"Ayrshire and Arran","Genital conditions",14,"",3857,36.3,""],
    [2952,2006,"Ayrshire and Arran","Limb conditions",23,"",3857,59.6,""],
    [2954,2006,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",10,"",3857,25.9,""],
    [2955,2006,"Borders","All major congenital conditions registerable by EUROCAT",14,"",1064,131.6,""],
    [2959,2006,"Borders","Congenital heart diseases (CHD)",5,"",1064,47,""],
    [2964,2006,"Borders","Kidney and urinary tract conditions",0,"",1064,0,""],
    [2965,2006,"Borders","Genital conditions",0,"",1064,0,""],
    [2969,2006,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",65,"",1469,442.5,""],
    [2972,2006,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1469,0,""],
    [2973,2006,"Dumfries and Galloway","Congenital heart diseases (CHD)",11,"",1469,74.9,""],
    [2976,2006,"Dumfries and Galloway","Gastro-intestinal conditions",6,"",1469,40.8,""],
    [2978,2006,"Dumfries and Galloway","Kidney and urinary tract conditions",15,"",1469,102.1,""],
    [2979,2006,"Dumfries and Galloway","Genital conditions",6,"",1469,40.8,""],
    [2980,2006,"Dumfries and Galloway","Limb conditions",8,"",1469,54.5,""],
    [2982,2006,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",12,"",1469,81.7,""],
    [2983,2006,"Fife","All major congenital conditions registerable by EUROCAT",100,"",3996,250.3,""],
    [2984,2006,"Fife","Nervous system conditions",12,"",3996,30,""],
    [2985,2006,"Fife","Eye conditions",5,"",3996,12.5,""],
    [2987,2006,"Fife","Congenital heart diseases (CHD)",21,"",3996,52.6,""],
    [2989,2006,"Fife","Oro-facial clefts",6,"",3996,15,""],
    [2990,2006,"Fife","Gastro-intestinal conditions",8,"",3996,20,""],
    [2992,2006,"Fife","Kidney and urinary tract conditions",11,"",3996,27.5,""],
    [2993,2006,"Fife","Genital conditions",11,"",3996,27.5,""],
    [2994,2006,"Fife","Limb conditions",17,"",3996,42.5,""],
    [2995,2006,"Fife","Other conditions/syndromes",5,"",3996,12.5,""],
    [2996,2006,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",19,"",3996,47.5,""],
    [2997,2006,"Forth Valley","All major congenital conditions registerable by EUROCAT",65,"",3189,203.8,""],
    [2998,2006,"Forth Valley","Nervous system conditions",6,"",3189,18.8,""],
    [3001,2006,"Forth Valley","Congenital heart diseases (CHD)",15,"",3189,47,""],
    [3004,2006,"Forth Valley","Gastro-intestinal conditions",5,"",3189,15.7,""],
    [3007,2006,"Forth Valley","Genital conditions",10,"",3189,31.4,""],
    [3008,2006,"Forth Valley","Limb conditions",10,"",3189,31.4,""],
    [3009,2006,"Forth Valley","Other conditions/syndromes",7,"",3189,22,""],
    [3010,2006,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",7,"",3189,22,""],
    [3011,2006,"Grampian","All major congenital conditions registerable by EUROCAT",230,"",5739,400.8,""],
    [3012,2006,"Grampian","Nervous system conditions",18,"",5739,31.4,""],
    [3013,2006,"Grampian","Eye conditions",5,"",5739,8.7,""],
    [3014,2006,"Grampian","Ear, face and neck conditions",0,"",5739,0,""],
    [3015,2006,"Grampian","Congenital heart diseases (CHD)",53,"",5739,92.4,""],
    [3017,2006,"Grampian","Oro-facial clefts",10,"",5739,17.4,""],
    [3018,2006,"Grampian","Gastro-intestinal conditions",18,"",5739,31.4,""],
    [3020,2006,"Grampian","Kidney and urinary tract conditions",25,"",5739,43.6,""],
    [3021,2006,"Grampian","Genital conditions",18,"",5739,31.4,""],
    [3022,2006,"Grampian","Limb conditions",49,"",5739,85.4,""],
    [3023,2006,"Grampian","Other conditions/syndromes",9,"",5739,15.7,""],
    [3024,2006,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",31,"",5739,54,""],
    [3025,2006,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",309,"",12253,252.2,""],
    [3026,2006,"Greater Glasgow and Clyde","Nervous system conditions",18,"",12253,14.7,""],
    [3027,2006,"Greater Glasgow and Clyde","Eye conditions",6,"",12253,4.9,""],
    [3029,2006,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",59,"",12253,48.2,""],
    [3030,2006,"Greater Glasgow and Clyde","Respiratory conditions",8,"",12253,6.5,""],
    [3031,2006,"Greater Glasgow and Clyde","Oro-facial clefts",13,"",12253,10.6,""],
    [3032,2006,"Greater Glasgow and Clyde","Gastro-intestinal conditions",31,"",12253,25.3,""],
    [3033,2006,"Greater Glasgow and Clyde","Abdominal wall defects",11,"",12253,9,""],
    [3034,2006,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",43,"",12253,35.1,""],
    [3035,2006,"Greater Glasgow and Clyde","Genital conditions",38,"",12253,31,""],
    [3036,2006,"Greater Glasgow and Clyde","Limb conditions",35,"",12253,28.6,""],
    [3037,2006,"Greater Glasgow and Clyde","Other conditions/syndromes",21,"",12253,17.1,""],
    [3038,2006,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",45,"",12253,36.7,""],
    [3039,2006,"Highland","All major congenital conditions registerable by EUROCAT",107,"",2978,359.3,""],
    [3040,2006,"Highland","Nervous system conditions",8,"",2978,26.9,""],
    [3043,2006,"Highland","Congenital heart diseases (CHD)",49,"",2978,164.5,""],
    [3044,2006,"Highland","Respiratory conditions",0,"",2978,0,""],
    [3045,2006,"Highland","Oro-facial clefts",6,"",2978,20.1,""],
    [3046,2006,"Highland","Gastro-intestinal conditions",5,"",2978,16.8,""],
    [3048,2006,"Highland","Kidney and urinary tract conditions",13,"",2978,43.7,""],
    [3050,2006,"Highland","Limb conditions",7,"",2978,23.5,""],
    [3051,2006,"Highland","Other conditions/syndromes",5,"",2978,16.8,""],
    [3052,2006,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",11,"",2978,36.9,""],
    [3053,2006,"Lanarkshire","All major congenital conditions registerable by EUROCAT",183,"",7569,241.8,""],
    [3054,2006,"Lanarkshire","Nervous system conditions",17,"",7569,22.5,""],
    [3055,2006,"Lanarkshire","Eye conditions",0,"",7569,0,""],
    [3057,2006,"Lanarkshire","Congenital heart diseases (CHD)",40,"",7569,52.8,""],
    [3058,2006,"Lanarkshire","Respiratory conditions",0,"",7569,0,""],
    [3059,2006,"Lanarkshire","Oro-facial clefts",12,"",7569,15.9,""],
    [3060,2006,"Lanarkshire","Gastro-intestinal conditions",25,"",7569,33,""],
    [3062,2006,"Lanarkshire","Kidney and urinary tract conditions",11,"",7569,14.5,""],
    [3063,2006,"Lanarkshire","Genital conditions",21,"",7569,27.7,""],
    [3064,2006,"Lanarkshire","Limb conditions",32,"",7569,42.3,""],
    [3065,2006,"Lanarkshire","Other conditions/syndromes",12,"",7569,15.9,""],
    [3066,2006,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",25,"",7569,33,""],
    [3067,2006,"Lothian","All major congenital conditions registerable by EUROCAT",325,"",9023,360.2,""],
    [3068,2006,"Lothian","Nervous system conditions",24,"",9023,26.6,""],
    [3069,2006,"Lothian","Eye conditions",9,"",9023,10,""],
    [3070,2006,"Lothian","Ear, face and neck conditions",15,"",9023,16.6,""],
    [3071,2006,"Lothian","Congenital heart diseases (CHD)",43,"",9023,47.7,""],
    [3072,2006,"Lothian","Respiratory conditions",6,"",9023,6.6,""],
    [3073,2006,"Lothian","Oro-facial clefts",11,"",9023,12.2,""],
    [3074,2006,"Lothian","Gastro-intestinal conditions",30,"",9023,33.2,""],
    [3076,2006,"Lothian","Kidney and urinary tract conditions",23,"",9023,25.5,""],
    [3077,2006,"Lothian","Genital conditions",50,"",9023,55.4,""],
    [3078,2006,"Lothian","Limb conditions",69,"",9023,76.5,""],
    [3079,2006,"Lothian","Other conditions/syndromes",16,"",9023,17.7,""],
    [3080,2006,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",56,"",9023,62.1,""],
    [3081,2006,"Orkney","All major congenital conditions registerable by EUROCAT",5,"",213,234.7,""],
    [3082,2006,"Orkney","Nervous system conditions",0,"",213,0,""],
    [3083,2006,"Orkney","Eye conditions",0,"",213,0,""],
    [3084,2006,"Orkney","Ear, face and neck conditions",0,"",213,0,""],
    [3085,2006,"Orkney","Congenital heart diseases (CHD)",0,"",213,0,""],
    [3086,2006,"Orkney","Respiratory conditions",0,"",213,0,""],
    [3088,2006,"Orkney","Gastro-intestinal conditions",0,"",213,0,""],
    [3089,2006,"Orkney","Abdominal wall defects",0,"",213,0,""],
    [3090,2006,"Orkney","Kidney and urinary tract conditions",0,"",213,0,""],
    [3092,2006,"Orkney","Limb conditions",0,"",213,0,""],
    [3093,2006,"Orkney","Other conditions/syndromes",0,"",213,0,""],
    [3095,2006,"Shetland","All major congenital conditions registerable by EUROCAT",14,"",274,510.9,""],
    [3096,2006,"Shetland","Nervous system conditions",0,"",274,0,""],
    [3097,2006,"Shetland","Eye conditions",0,"",274,0,""],
    [3098,2006,"Shetland","Ear, face and neck conditions",0,"",274,0,""],
    [3099,2006,"Shetland","Congenital heart diseases (CHD)",6,"",274,219,""],
    [3100,2006,"Shetland","Respiratory conditions",0,"",274,0,""],
    [3103,2006,"Shetland","Abdominal wall defects",0,"",274,0,""],
    [3108,2006,"Shetland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",6,"",274,219,""],
    [3109,2006,"Tayside","All major congenital conditions registerable by EUROCAT",119,"",4072,292.2,""],
    [3110,2006,"Tayside","Nervous system conditions",10,"",4072,24.6,""],
    [3113,2006,"Tayside","Congenital heart diseases (CHD)",40,"",4072,98.2,""],
    [3115,2006,"Tayside","Oro-facial clefts",5,"",4072,12.3,""],
    [3116,2006,"Tayside","Gastro-intestinal conditions",7,"",4072,17.2,""],
    [3118,2006,"Tayside","Kidney and urinary tract conditions",8,"",4072,19.6,""],
    [3119,2006,"Tayside","Genital conditions",11,"",4072,27,""],
    [3120,2006,"Tayside","Limb conditions",18,"",4072,44.2,""],
    [3121,2006,"Tayside","Other conditions/syndromes",9,"",4072,22.1,""],
    [3122,2006,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",4072,36.8,""],
    [3123,2006,"Total","All major congenital conditions registerable by EUROCAT",1652,"",56148,294.2,""],
    [3124,2006,"Total","Nervous system conditions",138,"",56148,24.6,""],
    [3125,2006,"Total","Eye conditions",34,"",56148,6.1,""],
    [3126,2006,"Total","Ear, face and neck conditions",27,"",56148,4.8,""],
    [3127,2006,"Total","Congenital heart diseases (CHD)",362,"",56148,64.5,""],
    [3128,2006,"Total","Respiratory conditions",31,"",56148,5.5,""],
    [3129,2006,"Total","Oro-facial clefts",79,"",56148,14.1,""],
    [3130,2006,"Total","Gastro-intestinal conditions",146,"",56148,26,""],
    [3131,2006,"Total","Abdominal wall defects",37,"",56148,6.6,""],
    [3132,2006,"Total","Kidney and urinary tract conditions",170,"",56148,30.3,""],
    [3133,2006,"Total","Genital conditions",184,"",56148,32.8,""],
    [3134,2006,"Total","Limb conditions",272,"",56148,48.4,""],
    [3135,2006,"Total","Other conditions/syndromes",95,"",56148,16.9,""],
    [3136,2006,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",243,"",56148,43.3,""],
    [3137,2006,"Western Isles","All major congenital conditions registerable by EUROCAT",5,"",277,180.5,""],
    [3139,2006,"Western Isles","Eye conditions",0,"",277,0,""],
    [3140,2006,"Western Isles","Ear, face and neck conditions",0,"",277,0,""],
    [3144,2006,"Western Isles","Gastro-intestinal conditions",0,"",277,0,""],
    [3145,2006,"Western Isles","Abdominal wall defects",0,"",277,0,""],
    [3146,2006,"Western Isles","Kidney and urinary tract conditions",0,"",277,0,""],
    [3147,2006,"Western Isles","Genital conditions",0,"",277,0,""],
    [3149,2006,"Western Isles","Other conditions/syndromes",0,"",277,0,""],
    [3150,2006,"Western Isles","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",277,0,""],
    [3151,2005,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",114,"",3645,312.8,""],
    [3152,2005,"Ayrshire and Arran","Nervous system conditions",14,"",3645,38.4,""],
    [3154,2005,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3645,0,""],
    [3155,2005,"Ayrshire and Arran","Congenital heart diseases (CHD)",35,"",3645,96,""],
    [3158,2005,"Ayrshire and Arran","Gastro-intestinal conditions",5,"",3645,13.7,""],
    [3160,2005,"Ayrshire and Arran","Kidney and urinary tract conditions",11,"",3645,30.2,""],
    [3161,2005,"Ayrshire and Arran","Genital conditions",11,"",3645,30.2,""],
    [3162,2005,"Ayrshire and Arran","Limb conditions",15,"",3645,41.2,""],
    [3163,2005,"Ayrshire and Arran","Other conditions/syndromes",6,"",3645,16.5,""],
    [3164,2005,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",23,"",3645,63.1,""],
    [3165,2005,"Borders","All major congenital conditions registerable by EUROCAT",22,"",1008,218.3,""],
    [3167,2005,"Borders","Eye conditions",0,"",1008,0,""],
    [3168,2005,"Borders","Ear, face and neck conditions",0,"",1008,0,""],
    [3169,2005,"Borders","Congenital heart diseases (CHD)",7,"",1008,69.4,""],
    [3170,2005,"Borders","Respiratory conditions",0,"",1008,0,""],
    [3174,2005,"Borders","Kidney and urinary tract conditions",0,"",1008,0,""],
    [3178,2005,"Borders","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",9,"",1008,89.3,""],
    [3179,2005,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",46,"",1398,329,""],
    [3182,2005,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1398,0,""],
    [3183,2005,"Dumfries and Galloway","Congenital heart diseases (CHD)",11,"",1398,78.7,""],
    [3186,2005,"Dumfries and Galloway","Gastro-intestinal conditions",0,"",1398,0,""],
    [3187,2005,"Dumfries and Galloway","Abdominal wall defects",0,"",1398,0,""],
    [3188,2005,"Dumfries and Galloway","Kidney and urinary tract conditions",10,"",1398,71.5,""],
    [3190,2005,"Dumfries and Galloway","Limb conditions",7,"",1398,50.1,""],
    [3191,2005,"Dumfries and Galloway","Other conditions/syndromes",0,"",1398,0,""],
    [3192,2005,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",10,"",1398,71.5,""],
    [3193,2005,"Fife","All major congenital conditions registerable by EUROCAT",90,"",3847,233.9,""],
    [3194,2005,"Fife","Nervous system conditions",11,"",3847,28.6,""],
    [3196,2005,"Fife","Ear, face and neck conditions",0,"",3847,0,""],
    [3197,2005,"Fife","Congenital heart diseases (CHD)",24,"",3847,62.4,""],
    [3199,2005,"Fife","Oro-facial clefts",7,"",3847,18.2,""],
    [3200,2005,"Fife","Gastro-intestinal conditions",8,"",3847,20.8,""],
    [3202,2005,"Fife","Kidney and urinary tract conditions",12,"",3847,31.2,""],
    [3203,2005,"Fife","Genital conditions",5,"",3847,13,""],
    [3204,2005,"Fife","Limb conditions",14,"",3847,36.4,""],
    [3206,2005,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",3847,41.6,""],
    [3207,2005,"Forth Valley","All major congenital conditions registerable by EUROCAT",101,"",3173,318.3,""],
    [3208,2005,"Forth Valley","Nervous system conditions",10,"",3173,31.5,""],
    [3211,2005,"Forth Valley","Congenital heart diseases (CHD)",17,"",3173,53.6,""],
    [3212,2005,"Forth Valley","Respiratory conditions",0,"",3173,0,""],
    [3213,2005,"Forth Valley","Oro-facial clefts",8,"",3173,25.2,""],
    [3214,2005,"Forth Valley","Gastro-intestinal conditions",13,"",3173,41,""],
    [3217,2005,"Forth Valley","Genital conditions",15,"",3173,47.3,""],
    [3218,2005,"Forth Valley","Limb conditions",17,"",3173,53.6,""],
    [3219,2005,"Forth Valley","Other conditions/syndromes",5,"",3173,15.8,""],
    [3220,2005,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",22,"",3173,69.3,""],
    [3221,2005,"Grampian","All major congenital conditions registerable by EUROCAT",227,"",5436,417.6,""],
    [3222,2005,"Grampian","Nervous system conditions",20,"",5436,36.8,""],
    [3225,2005,"Grampian","Congenital heart diseases (CHD)",66,"",5436,121.4,""],
    [3226,2005,"Grampian","Respiratory conditions",0,"",5436,0,""],
    [3227,2005,"Grampian","Oro-facial clefts",11,"",5436,20.2,""],
    [3228,2005,"Grampian","Gastro-intestinal conditions",16,"",5436,29.4,""],
    [3230,2005,"Grampian","Kidney and urinary tract conditions",13,"",5436,23.9,""],
    [3231,2005,"Grampian","Genital conditions",28,"",5436,51.5,""],
    [3232,2005,"Grampian","Limb conditions",42,"",5436,77.3,""],
    [3233,2005,"Grampian","Other conditions/syndromes",7,"",5436,12.9,""],
    [3234,2005,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",24,"",5436,44.2,""],
    [3235,2005,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",319,"",12367,257.9,""],
    [3236,2005,"Greater Glasgow and Clyde","Nervous system conditions",24,"",12367,19.4,""],
    [3237,2005,"Greater Glasgow and Clyde","Eye conditions",6,"",12367,4.9,""],
    [3239,2005,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",72,"",12367,58.2,""],
    [3240,2005,"Greater Glasgow and Clyde","Respiratory conditions",18,"",12367,14.6,""],
    [3241,2005,"Greater Glasgow and Clyde","Oro-facial clefts",21,"",12367,17,""],
    [3242,2005,"Greater Glasgow and Clyde","Gastro-intestinal conditions",34,"",12367,27.5,""],
    [3243,2005,"Greater Glasgow and Clyde","Abdominal wall defects",11,"",12367,8.9,""],
    [3244,2005,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",29,"",12367,23.4,""],
    [3245,2005,"Greater Glasgow and Clyde","Genital conditions",35,"",12367,28.3,""],
    [3246,2005,"Greater Glasgow and Clyde","Limb conditions",38,"",12367,30.7,""],
    [3247,2005,"Greater Glasgow and Clyde","Other conditions/syndromes",17,"",12367,13.7,""],
    [3248,2005,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",39,"",12367,31.5,""],
    [3249,2005,"Highland","All major congenital conditions registerable by EUROCAT",117,"",2990,391.3,""],
    [3250,2005,"Highland","Nervous system conditions",10,"",2990,33.4,""],
    [3253,2005,"Highland","Congenital heart diseases (CHD)",42,"",2990,140.5,""],
    [3255,2005,"Highland","Oro-facial clefts",8,"",2990,26.8,""],
    [3256,2005,"Highland","Gastro-intestinal conditions",9,"",2990,30.1,""],
    [3258,2005,"Highland","Kidney and urinary tract conditions",9,"",2990,30.1,""],
    [3259,2005,"Highland","Genital conditions",17,"",2990,56.9,""],
    [3260,2005,"Highland","Limb conditions",6,"",2990,20.1,""],
    [3261,2005,"Highland","Other conditions/syndromes",6,"",2990,20.1,""],
    [3262,2005,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",2990,53.5,""],
    [3263,2005,"Lanarkshire","All major congenital conditions registerable by EUROCAT",146,"",7228,202,""],
    [3264,2005,"Lanarkshire","Nervous system conditions",21,"",7228,29.1,""],
    [3267,2005,"Lanarkshire","Congenital heart diseases (CHD)",33,"",7228,45.7,""],
    [3268,2005,"Lanarkshire","Respiratory conditions",6,"",7228,8.3,""],
    [3269,2005,"Lanarkshire","Oro-facial clefts",9,"",7228,12.5,""],
    [3270,2005,"Lanarkshire","Gastro-intestinal conditions",15,"",7228,20.8,""],
    [3272,2005,"Lanarkshire","Kidney and urinary tract conditions",10,"",7228,13.8,""],
    [3273,2005,"Lanarkshire","Genital conditions",14,"",7228,19.4,""],
    [3274,2005,"Lanarkshire","Limb conditions",19,"",7228,26.3,""],
    [3275,2005,"Lanarkshire","Other conditions/syndromes",8,"",7228,11.1,""],
    [3276,2005,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",21,"",7228,29.1,""],
    [3277,2005,"Lothian","All major congenital conditions registerable by EUROCAT",386,"",8777,439.8,""],
    [3278,2005,"Lothian","Nervous system conditions",29,"",8777,33,""],
    [3279,2005,"Lothian","Eye conditions",17,"",8777,19.4,""],
    [3280,2005,"Lothian","Ear, face and neck conditions",10,"",8777,11.4,""],
    [3281,2005,"Lothian","Congenital heart diseases (CHD)",43,"",8777,49,""],
    [3283,2005,"Lothian","Oro-facial clefts",23,"",8777,26.2,""],
    [3284,2005,"Lothian","Gastro-intestinal conditions",37,"",8777,42.2,""],
    [3285,2005,"Lothian","Abdominal wall defects",6,"",8777,6.8,""],
    [3286,2005,"Lothian","Kidney and urinary tract conditions",35,"",8777,39.9,""],
    [3287,2005,"Lothian","Genital conditions",74,"",8777,84.3,""],
    [3288,2005,"Lothian","Limb conditions",72,"",8777,82,""],
    [3289,2005,"Lothian","Other conditions/syndromes",9,"",8777,10.3,""],
    [3290,2005,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",59,"",8777,67.2,""],
    [3293,2005,"Orkney","Eye conditions",0,"",180,0,""],
    [3294,2005,"Orkney","Ear, face and neck conditions",0,"",180,0,""],
    [3295,2005,"Orkney","Congenital heart diseases (CHD)",0,"",180,0,""],
    [3296,2005,"Orkney","Respiratory conditions",0,"",180,0,""],
    [3298,2005,"Orkney","Gastro-intestinal conditions",0,"",180,0,""],
    [3299,2005,"Orkney","Abdominal wall defects",0,"",180,0,""],
    [3300,2005,"Orkney","Kidney and urinary tract conditions",0,"",180,0,""],
    [3301,2005,"Orkney","Genital conditions",0,"",180,0,""],
    [3302,2005,"Orkney","Limb conditions",0,"",180,0,""],
    [3303,2005,"Orkney","Other conditions/syndromes",0,"",180,0,""],
    [3305,2005,"Shetland","All major congenital conditions registerable by EUROCAT",6,"",223,269.1,""],
    [3306,2005,"Shetland","Nervous system conditions",0,"",223,0,""],
    [3307,2005,"Shetland","Eye conditions",0,"",223,0,""],
    [3308,2005,"Shetland","Ear, face and neck conditions",0,"",223,0,""],
    [3310,2005,"Shetland","Respiratory conditions",0,"",223,0,""],
    [3311,2005,"Shetland","Oro-facial clefts",0,"",223,0,""],
    [3312,2005,"Shetland","Gastro-intestinal conditions",0,"",223,0,""],
    [3313,2005,"Shetland","Abdominal wall defects",0,"",223,0,""],
    [3315,2005,"Shetland","Genital conditions",0,"",223,0,""],
    [3316,2005,"Shetland","Limb conditions",0,"",223,0,""],
    [3317,2005,"Shetland","Other conditions/syndromes",0,"",223,0,""],
    [3319,2005,"Tayside","All major congenital conditions registerable by EUROCAT",96,"",3970,241.8,""],
    [3320,2005,"Tayside","Nervous system conditions",12,"",3970,30.2,""],
    [3322,2005,"Tayside","Ear, face and neck conditions",0,"",3970,0,""],
    [3323,2005,"Tayside","Congenital heart diseases (CHD)",22,"",3970,55.4,""],
    [3326,2005,"Tayside","Gastro-intestinal conditions",10,"",3970,25.2,""],
    [3328,2005,"Tayside","Kidney and urinary tract conditions",8,"",3970,20.2,""],
    [3329,2005,"Tayside","Genital conditions",7,"",3970,17.6,""],
    [3330,2005,"Tayside","Limb conditions",9,"",3970,22.7,""],
    [3332,2005,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",22,"",3970,55.4,""],
    [3333,2005,"Total","All major congenital conditions registerable by EUROCAT",1678,"",54684,306.9,""],
    [3334,2005,"Total","Nervous system conditions",157,"",54684,28.7,""],
    [3335,2005,"Total","Eye conditions",43,"",54684,7.9,""],
    [3336,2005,"Total","Ear, face and neck conditions",19,"",54684,3.5,""],
    [3337,2005,"Total","Congenital heart diseases (CHD)",376,"",54684,68.8,""],
    [3338,2005,"Total","Respiratory conditions",35,"",54684,6.4,""],
    [3339,2005,"Total","Oro-facial clefts",99,"",54684,18.1,""],
    [3340,2005,"Total","Gastro-intestinal conditions",150,"",54684,27.4,""],
    [3341,2005,"Total","Abdominal wall defects",38,"",54684,6.9,""],
    [3342,2005,"Total","Kidney and urinary tract conditions",141,"",54684,25.8,""],
    [3343,2005,"Total","Genital conditions",211,"",54684,38.6,""],
    [3344,2005,"Total","Limb conditions",243,"",54684,44.4,""],
    [3345,2005,"Total","Other conditions/syndromes",64,"",54684,11.7,""],
    [3346,2005,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",265,"",54684,48.5,""],
    [3348,2005,"Western Isles","Nervous system conditions",0,"",232,0,""],
    [3349,2005,"Western Isles","Eye conditions",0,"",232,0,""],
    [3350,2005,"Western Isles","Ear, face and neck conditions",0,"",232,0,""],
    [3352,2005,"Western Isles","Respiratory conditions",0,"",232,0,""],
    [3354,2005,"Western Isles","Gastro-intestinal conditions",0,"",232,0,""],
    [3355,2005,"Western Isles","Abdominal wall defects",0,"",232,0,""],
    [3356,2005,"Western Isles","Kidney and urinary tract conditions",0,"",232,0,""],
    [3357,2005,"Western Isles","Genital conditions",0,"",232,0,""],
    [3358,2005,"Western Isles","Limb conditions",0,"",232,0,""],
    [3359,2005,"Western Isles","Other conditions/syndromes",0,"",232,0,""],
    [3360,2005,"Western Isles","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",232,0,""],
    [3361,2004,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",132,"",3727,354.2,""],
    [3362,2004,"Ayrshire and Arran","Nervous system conditions",10,"",3727,26.8,""],
    [3365,2004,"Ayrshire and Arran","Congenital heart diseases (CHD)",36,"",3727,96.6,""],
    [3366,2004,"Ayrshire and Arran","Respiratory conditions",0,"",3727,0,""],
    [3367,2004,"Ayrshire and Arran","Oro-facial clefts",6,"",3727,16.1,""],
    [3368,2004,"Ayrshire and Arran","Gastro-intestinal conditions",14,"",3727,37.6,""],
    [3370,2004,"Ayrshire and Arran","Kidney and urinary tract conditions",16,"",3727,42.9,""],
    [3371,2004,"Ayrshire and Arran","Genital conditions",15,"",3727,40.2,""],
    [3372,2004,"Ayrshire and Arran","Limb conditions",13,"",3727,34.9,""],
    [3374,2004,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",29,"",3727,77.8,""],
    [3375,2004,"Borders","All major congenital conditions registerable by EUROCAT",24,"",1023,234.6,""],
    [3377,2004,"Borders","Eye conditions",0,"",1023,0,""],
    [3378,2004,"Borders","Ear, face and neck conditions",0,"",1023,0,""],
    [3379,2004,"Borders","Congenital heart diseases (CHD)",6,"",1023,58.7,""],
    [3380,2004,"Borders","Respiratory conditions",0,"",1023,0,""],
    [3383,2004,"Borders","Abdominal wall defects",0,"",1023,0,""],
    [3384,2004,"Borders","Kidney and urinary tract conditions",0,"",1023,0,""],
    [3389,2004,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",41,"",1436,285.5,""],
    [3391,2004,"Dumfries and Galloway","Eye conditions",0,"",1436,0,""],
    [3393,2004,"Dumfries and Galloway","Congenital heart diseases (CHD)",11,"",1436,76.6,""],
    [3397,2004,"Dumfries and Galloway","Abdominal wall defects",0,"",1436,0,""],
    [3398,2004,"Dumfries and Galloway","Kidney and urinary tract conditions",8,"",1436,55.7,""],
    [3401,2004,"Dumfries and Galloway","Other conditions/syndromes",0,"",1436,0,""],
    [3402,2004,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",9,"",1436,62.7,""],
    [3403,2004,"Fife","All major congenital conditions registerable by EUROCAT",97,"",3795,255.6,""],
    [3404,2004,"Fife","Nervous system conditions",18,"",3795,47.4,""],
    [3406,2004,"Fife","Ear, face and neck conditions",0,"",3795,0,""],
    [3407,2004,"Fife","Congenital heart diseases (CHD)",20,"",3795,52.7,""],
    [3409,2004,"Fife","Oro-facial clefts",5,"",3795,13.2,""],
    [3410,2004,"Fife","Gastro-intestinal conditions",5,"",3795,13.2,""],
    [3412,2004,"Fife","Kidney and urinary tract conditions",7,"",3795,18.4,""],
    [3413,2004,"Fife","Genital conditions",8,"",3795,21.1,""],
    [3414,2004,"Fife","Limb conditions",16,"",3795,42.2,""],
    [3416,2004,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",9,"",3795,23.7,""],
    [3417,2004,"Forth Valley","All major congenital conditions registerable by EUROCAT",82,"",3197,256.5,""],
    [3418,2004,"Forth Valley","Nervous system conditions",8,"",3197,25,""],
    [3419,2004,"Forth Valley","Eye conditions",0,"",3197,0,""],
    [3420,2004,"Forth Valley","Ear, face and neck conditions",0,"",3197,0,""],
    [3421,2004,"Forth Valley","Congenital heart diseases (CHD)",14,"",3197,43.8,""],
    [3422,2004,"Forth Valley","Respiratory conditions",0,"",3197,0,""],
    [3423,2004,"Forth Valley","Oro-facial clefts",7,"",3197,21.9,""],
    [3427,2004,"Forth Valley","Genital conditions",17,"",3197,53.2,""],
    [3428,2004,"Forth Valley","Limb conditions",13,"",3197,40.7,""],
    [3429,2004,"Forth Valley","Other conditions/syndromes",0,"",3197,0,""],
    [3430,2004,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",14,"",3197,43.8,""],
    [3431,2004,"Grampian","All major congenital conditions registerable by EUROCAT",280,"",5347,523.7,""],
    [3432,2004,"Grampian","Nervous system conditions",18,"",5347,33.7,""],
    [3434,2004,"Grampian","Ear, face and neck conditions",0,"",5347,0,""],
    [3435,2004,"Grampian","Congenital heart diseases (CHD)",77,"",5347,144,""],
    [3437,2004,"Grampian","Oro-facial clefts",9,"",5347,16.8,""],
    [3438,2004,"Grampian","Gastro-intestinal conditions",14,"",5347,26.2,""],
    [3440,2004,"Grampian","Kidney and urinary tract conditions",15,"",5347,28.1,""],
    [3441,2004,"Grampian","Genital conditions",51,"",5347,95.4,""],
    [3442,2004,"Grampian","Limb conditions",54,"",5347,101,""],
    [3443,2004,"Grampian","Other conditions/syndromes",13,"",5347,24.3,""],
    [3444,2004,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",47,"",5347,87.9,""],
    [3445,2004,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",353,"",12436,283.9,""],
    [3446,2004,"Greater Glasgow and Clyde","Nervous system conditions",33,"",12436,26.5,""],
    [3447,2004,"Greater Glasgow and Clyde","Eye conditions",5,"",12436,4,""],
    [3449,2004,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",73,"",12436,58.7,""],
    [3450,2004,"Greater Glasgow and Clyde","Respiratory conditions",13,"",12436,10.5,""],
    [3451,2004,"Greater Glasgow and Clyde","Oro-facial clefts",19,"",12436,15.3,""],
    [3452,2004,"Greater Glasgow and Clyde","Gastro-intestinal conditions",26,"",12436,20.9,""],
    [3453,2004,"Greater Glasgow and Clyde","Abdominal wall defects",7,"",12436,5.6,""],
    [3454,2004,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",23,"",12436,18.5,""],
    [3455,2004,"Greater Glasgow and Clyde","Genital conditions",38,"",12436,30.6,""],
    [3456,2004,"Greater Glasgow and Clyde","Limb conditions",44,"",12436,35.4,""],
    [3457,2004,"Greater Glasgow and Clyde","Other conditions/syndromes",19,"",12436,15.3,""],
    [3458,2004,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",58,"",12436,46.6,""],
    [3459,2004,"Highland","All major congenital conditions registerable by EUROCAT",105,"",2974,353.1,""],
    [3460,2004,"Highland","Nervous system conditions",6,"",2974,20.2,""],
    [3462,2004,"Highland","Ear, face and neck conditions",0,"",2974,0,""],
    [3463,2004,"Highland","Congenital heart diseases (CHD)",48,"",2974,161.4,""],
    [3464,2004,"Highland","Respiratory conditions",0,"",2974,0,""],
    [3465,2004,"Highland","Oro-facial clefts",7,"",2974,23.5,""],
    [3466,2004,"Highland","Gastro-intestinal conditions",7,"",2974,23.5,""],
    [3467,2004,"Highland","Abdominal wall defects",0,"",2974,0,""],
    [3468,2004,"Highland","Kidney and urinary tract conditions",8,"",2974,26.9,""],
    [3469,2004,"Highland","Genital conditions",11,"",2974,37,""],
    [3470,2004,"Highland","Limb conditions",12,"",2974,40.3,""],
    [3472,2004,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",14,"",2974,47.1,""],
    [3473,2004,"Lanarkshire","All major congenital conditions registerable by EUROCAT",130,"",7390,175.9,""],
    [3474,2004,"Lanarkshire","Nervous system conditions",16,"",7390,21.7,""],
    [3477,2004,"Lanarkshire","Congenital heart diseases (CHD)",44,"",7390,59.5,""],
    [3478,2004,"Lanarkshire","Respiratory conditions",6,"",7390,8.1,""],
    [3479,2004,"Lanarkshire","Oro-facial clefts",8,"",7390,10.8,""],
    [3480,2004,"Lanarkshire","Gastro-intestinal conditions",18,"",7390,24.4,""],
    [3482,2004,"Lanarkshire","Kidney and urinary tract conditions",6,"",7390,8.1,""],
    [3483,2004,"Lanarkshire","Genital conditions",7,"",7390,9.5,""],
    [3484,2004,"Lanarkshire","Limb conditions",12,"",7390,16.2,""],
    [3485,2004,"Lanarkshire","Other conditions/syndromes",14,"",7390,18.9,""],
    [3486,2004,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",17,"",7390,23,""],
    [3487,2004,"Lothian","All major congenital conditions registerable by EUROCAT",358,"",8488,421.8,""],
    [3488,2004,"Lothian","Nervous system conditions",25,"",8488,29.5,""],
    [3489,2004,"Lothian","Eye conditions",9,"",8488,10.6,""],
    [3491,2004,"Lothian","Congenital heart diseases (CHD)",60,"",8488,70.7,""],
    [3492,2004,"Lothian","Respiratory conditions",6,"",8488,7.1,""],
    [3493,2004,"Lothian","Oro-facial clefts",21,"",8488,24.7,""],
    [3494,2004,"Lothian","Gastro-intestinal conditions",32,"",8488,37.7,""],
    [3495,2004,"Lothian","Abdominal wall defects",6,"",8488,7.1,""],
    [3496,2004,"Lothian","Kidney and urinary tract conditions",21,"",8488,24.7,""],
    [3497,2004,"Lothian","Genital conditions",50,"",8488,58.9,""],
    [3498,2004,"Lothian","Limb conditions",91,"",8488,107.2,""],
    [3499,2004,"Lothian","Other conditions/syndromes",17,"",8488,20,""],
    [3500,2004,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",59,"",8488,69.5,""],
    [3501,2004,"Orkney","All major congenital conditions registerable by EUROCAT",6,"",174,344.8,""],
    [3502,2004,"Orkney","Nervous system conditions",0,"",174,0,""],
    [3503,2004,"Orkney","Eye conditions",0,"",174,0,""],
    [3504,2004,"Orkney","Ear, face and neck conditions",0,"",174,0,""],
    [3506,2004,"Orkney","Respiratory conditions",0,"",174,0,""],
    [3507,2004,"Orkney","Oro-facial clefts",0,"",174,0,""],
    [3508,2004,"Orkney","Gastro-intestinal conditions",0,"",174,0,""],
    [3509,2004,"Orkney","Abdominal wall defects",0,"",174,0,""],
    [3513,2004,"Orkney","Other conditions/syndromes",0,"",174,0,""],
    [3514,2004,"Orkney","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",174,0,""],
    [3516,2004,"Shetland","Nervous system conditions",0,"",233,0,""],
    [3517,2004,"Shetland","Eye conditions",0,"",233,0,""],
    [3518,2004,"Shetland","Ear, face and neck conditions",0,"",233,0,""],
    [3519,2004,"Shetland","Congenital heart diseases (CHD)",0,"",233,0,""],
    [3520,2004,"Shetland","Respiratory conditions",0,"",233,0,""],
    [3521,2004,"Shetland","Oro-facial clefts",0,"",233,0,""],
    [3522,2004,"Shetland","Gastro-intestinal conditions",0,"",233,0,""],
    [3523,2004,"Shetland","Abdominal wall defects",0,"",233,0,""],
    [3525,2004,"Shetland","Genital conditions",0,"",233,0,""],
    [3527,2004,"Shetland","Other conditions/syndromes",0,"",233,0,""],
    [3529,2004,"Tayside","All major congenital conditions registerable by EUROCAT",121,"",3902,310.1,""],
    [3530,2004,"Tayside","Nervous system conditions",10,"",3902,25.6,""],
    [3532,2004,"Tayside","Ear, face and neck conditions",0,"",3902,0,""],
    [3533,2004,"Tayside","Congenital heart diseases (CHD)",23,"",3902,58.9,""],
    [3535,2004,"Tayside","Oro-facial clefts",7,"",3902,17.9,""],
    [3536,2004,"Tayside","Gastro-intestinal conditions",11,"",3902,28.2,""],
    [3538,2004,"Tayside","Kidney and urinary tract conditions",9,"",3902,23.1,""],
    [3539,2004,"Tayside","Genital conditions",12,"",3902,30.8,""],
    [3540,2004,"Tayside","Limb conditions",20,"",3902,51.3,""],
    [3542,2004,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",30,"",3902,76.9,""],
    [3543,2004,"Total","All major congenital conditions registerable by EUROCAT",1738,"",54522,318.8,""],
    [3544,2004,"Total","Nervous system conditions",153,"",54522,28.1,""],
    [3545,2004,"Total","Eye conditions",27,"",54522,5,""],
    [3546,2004,"Total","Ear, face and neck conditions",7,"",54522,1.3,""],
    [3547,2004,"Total","Congenital heart diseases (CHD)",415,"",54522,76.1,""],
    [3548,2004,"Total","Respiratory conditions",36,"",54522,6.6,""],
    [3549,2004,"Total","Oro-facial clefts",94,"",54522,17.2,""],
    [3550,2004,"Total","Gastro-intestinal conditions",138,"",54522,25.3,""],
    [3551,2004,"Total","Abdominal wall defects",27,"",54522,5,""],
    [3552,2004,"Total","Kidney and urinary tract conditions",119,"",54522,21.8,""],
    [3553,2004,"Total","Genital conditions",215,"",54522,39.4,""],
    [3554,2004,"Total","Limb conditions",286,"",54522,52.5,""],
    [3555,2004,"Total","Other conditions/syndromes",76,"",54522,13.9,""],
    [3556,2004,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",293,"",54522,53.7,""],
    [3559,2004,"Western Isles","Eye conditions",0,"",223,0,""],
    [3560,2004,"Western Isles","Ear, face and neck conditions",0,"",223,0,""],
    [3562,2004,"Western Isles","Respiratory conditions",0,"",223,0,""],
    [3563,2004,"Western Isles","Oro-facial clefts",0,"",223,0,""],
    [3565,2004,"Western Isles","Abdominal wall defects",0,"",223,0,""],
    [3566,2004,"Western Isles","Kidney and urinary tract conditions",0,"",223,0,""],
    [3567,2004,"Western Isles","Genital conditions",0,"",223,0,""],
    [3568,2004,"Western Isles","Limb conditions",0,"",223,0,""],
    [3569,2004,"Western Isles","Other conditions/syndromes",0,"",223,0,""],
    [3571,2003,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",132,"",3583,368.4,""],
    [3572,2003,"Ayrshire and Arran","Nervous system conditions",13,"",3583,36.3,""],
    [3574,2003,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3583,0,""],
    [3575,2003,"Ayrshire and Arran","Congenital heart diseases (CHD)",30,"",3583,83.7,""],
    [3576,2003,"Ayrshire and Arran","Respiratory conditions",0,"",3583,0,""],
    [3577,2003,"Ayrshire and Arran","Oro-facial clefts",8,"",3583,22.3,""],
    [3578,2003,"Ayrshire and Arran","Gastro-intestinal conditions",9,"",3583,25.1,""],
    [3579,2003,"Ayrshire and Arran","Abdominal wall defects",6,"",3583,16.7,""],
    [3580,2003,"Ayrshire and Arran","Kidney and urinary tract conditions",22,"",3583,61.4,""],
    [3581,2003,"Ayrshire and Arran","Genital conditions",17,"",3583,47.4,""],
    [3582,2003,"Ayrshire and Arran","Limb conditions",18,"",3583,50.2,""],
    [3583,2003,"Ayrshire and Arran","Other conditions/syndromes",9,"",3583,25.1,""],
    [3584,2003,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",22,"",3583,61.4,""],
    [3585,2003,"Borders","All major congenital conditions registerable by EUROCAT",18,"",1003,179.5,""],
    [3586,2003,"Borders","Nervous system conditions",6,"",1003,59.8,""],
    [3587,2003,"Borders","Eye conditions",0,"",1003,0,""],
    [3588,2003,"Borders","Ear, face and neck conditions",0,"",1003,0,""],
    [3589,2003,"Borders","Congenital heart diseases (CHD)",7,"",1003,69.8,""],
    [3590,2003,"Borders","Respiratory conditions",0,"",1003,0,""],
    [3593,2003,"Borders","Abdominal wall defects",0,"",1003,0,""],
    [3597,2003,"Borders","Other conditions/syndromes",0,"",1003,0,""],
    [3599,2003,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",47,"",1298,362.1,""],
    [3600,2003,"Dumfries and Galloway","Nervous system conditions",5,"",1298,38.5,""],
    [3603,2003,"Dumfries and Galloway","Congenital heart diseases (CHD)",8,"",1298,61.6,""],
    [3604,2003,"Dumfries and Galloway","Respiratory conditions",0,"",1298,0,""],
    [3605,2003,"Dumfries and Galloway","Oro-facial clefts",5,"",1298,38.5,""],
    [3607,2003,"Dumfries and Galloway","Abdominal wall defects",0,"",1298,0,""],
    [3608,2003,"Dumfries and Galloway","Kidney and urinary tract conditions",7,"",1298,53.9,""],
    [3609,2003,"Dumfries and Galloway","Genital conditions",10,"",1298,77,""],
    [3610,2003,"Dumfries and Galloway","Limb conditions",6,"",1298,46.2,""],
    [3612,2003,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",6,"",1298,46.2,""],
    [3613,2003,"Fife","All major congenital conditions registerable by EUROCAT",91,"",3644,249.7,""],
    [3614,2003,"Fife","Nervous system conditions",14,"",3644,38.4,""],
    [3615,2003,"Fife","Eye conditions",5,"",3644,13.7,""],
    [3617,2003,"Fife","Congenital heart diseases (CHD)",13,"",3644,35.7,""],
    [3620,2003,"Fife","Gastro-intestinal conditions",8,"",3644,22,""],
    [3622,2003,"Fife","Kidney and urinary tract conditions",15,"",3644,41.2,""],
    [3623,2003,"Fife","Genital conditions",9,"",3644,24.7,""],
    [3624,2003,"Fife","Limb conditions",10,"",3644,27.4,""],
    [3625,2003,"Fife","Other conditions/syndromes",6,"",3644,16.5,""],
    [3626,2003,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",3644,43.9,""],
    [3627,2003,"Forth Valley","All major congenital conditions registerable by EUROCAT",62,"",2929,211.7,""],
    [3628,2003,"Forth Valley","Nervous system conditions",14,"",2929,47.8,""],
    [3629,2003,"Forth Valley","Eye conditions",0,"",2929,0,""],
    [3630,2003,"Forth Valley","Ear, face and neck conditions",0,"",2929,0,""],
    [3631,2003,"Forth Valley","Congenital heart diseases (CHD)",13,"",2929,44.4,""],
    [3637,2003,"Forth Valley","Genital conditions",5,"",2929,17.1,""],
    [3638,2003,"Forth Valley","Limb conditions",11,"",2929,37.6,""],
    [3640,2003,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",12,"",2929,41,""],
    [3641,2003,"Grampian","All major congenital conditions registerable by EUROCAT",241,"",5192,464.2,""],
    [3642,2003,"Grampian","Nervous system conditions",12,"",5192,23.1,""],
    [3645,2003,"Grampian","Congenital heart diseases (CHD)",75,"",5192,144.5,""],
    [3647,2003,"Grampian","Oro-facial clefts",7,"",5192,13.5,""],
    [3648,2003,"Grampian","Gastro-intestinal conditions",13,"",5192,25,""],
    [3650,2003,"Grampian","Kidney and urinary tract conditions",16,"",5192,30.8,""],
    [3651,2003,"Grampian","Genital conditions",22,"",5192,42.4,""],
    [3652,2003,"Grampian","Limb conditions",48,"",5192,92.4,""],
    [3653,2003,"Grampian","Other conditions/syndromes",8,"",5192,15.4,""],
    [3654,2003,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",45,"",5192,86.7,""],
    [3655,2003,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",329,"",12013,273.9,""],
    [3656,2003,"Greater Glasgow and Clyde","Nervous system conditions",35,"",12013,29.1,""],
    [3657,2003,"Greater Glasgow and Clyde","Eye conditions",11,"",12013,9.2,""],
    [3659,2003,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",60,"",12013,49.9,""],
    [3660,2003,"Greater Glasgow and Clyde","Respiratory conditions",15,"",12013,12.5,""],
    [3661,2003,"Greater Glasgow and Clyde","Oro-facial clefts",17,"",12013,14.2,""],
    [3662,2003,"Greater Glasgow and Clyde","Gastro-intestinal conditions",24,"",12013,20,""],
    [3663,2003,"Greater Glasgow and Clyde","Abdominal wall defects",10,"",12013,8.3,""],
    [3664,2003,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",41,"",12013,34.1,""],
    [3665,2003,"Greater Glasgow and Clyde","Genital conditions",41,"",12013,34.1,""],
    [3666,2003,"Greater Glasgow and Clyde","Limb conditions",40,"",12013,33.3,""],
    [3667,2003,"Greater Glasgow and Clyde","Other conditions/syndromes",21,"",12013,17.5,""],
    [3668,2003,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",49,"",12013,40.8,""],
    [3669,2003,"Highland","All major congenital conditions registerable by EUROCAT",92,"",2824,325.8,""],
    [3670,2003,"Highland","Nervous system conditions",6,"",2824,21.2,""],
    [3672,2003,"Highland","Ear, face and neck conditions",0,"",2824,0,""],
    [3673,2003,"Highland","Congenital heart diseases (CHD)",32,"",2824,113.3,""],
    [3675,2003,"Highland","Oro-facial clefts",5,"",2824,17.7,""],
    [3676,2003,"Highland","Gastro-intestinal conditions",7,"",2824,24.8,""],
    [3677,2003,"Highland","Abdominal wall defects",0,"",2824,0,""],
    [3678,2003,"Highland","Kidney and urinary tract conditions",8,"",2824,28.3,""],
    [3679,2003,"Highland","Genital conditions",9,"",2824,31.9,""],
    [3680,2003,"Highland","Limb conditions",16,"",2824,56.7,""],
    [3682,2003,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",2824,53.1,""],
    [3683,2003,"Lanarkshire","All major congenital conditions registerable by EUROCAT",152,"",6902,220.2,""],
    [3684,2003,"Lanarkshire","Nervous system conditions",15,"",6902,21.7,""],
    [3686,2003,"Lanarkshire","Ear, face and neck conditions",0,"",6902,0,""],
    [3687,2003,"Lanarkshire","Congenital heart diseases (CHD)",40,"",6902,58,""],
    [3688,2003,"Lanarkshire","Respiratory conditions",0,"",6902,0,""],
    [3689,2003,"Lanarkshire","Oro-facial clefts",9,"",6902,13,""],
    [3690,2003,"Lanarkshire","Gastro-intestinal conditions",16,"",6902,23.2,""],
    [3692,2003,"Lanarkshire","Kidney and urinary tract conditions",15,"",6902,21.7,""],
    [3693,2003,"Lanarkshire","Genital conditions",12,"",6902,17.4,""],
    [3694,2003,"Lanarkshire","Limb conditions",19,"",6902,27.5,""],
    [3695,2003,"Lanarkshire","Other conditions/syndromes",13,"",6902,18.8,""],
    [3696,2003,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",30,"",6902,43.5,""],
    [3697,2003,"Lothian","All major congenital conditions registerable by EUROCAT",278,"",8436,329.5,""],
    [3698,2003,"Lothian","Nervous system conditions",40,"",8436,47.4,""],
    [3699,2003,"Lothian","Eye conditions",7,"",8436,8.3,""],
    [3700,2003,"Lothian","Ear, face and neck conditions",7,"",8436,8.3,""],
    [3701,2003,"Lothian","Congenital heart diseases (CHD)",38,"",8436,45,""],
    [3702,2003,"Lothian","Respiratory conditions",5,"",8436,5.9,""],
    [3703,2003,"Lothian","Oro-facial clefts",14,"",8436,16.6,""],
    [3704,2003,"Lothian","Gastro-intestinal conditions",34,"",8436,40.3,""],
    [3706,2003,"Lothian","Kidney and urinary tract conditions",5,"",8436,5.9,""],
    [3707,2003,"Lothian","Genital conditions",44,"",8436,52.2,""],
    [3708,2003,"Lothian","Limb conditions",63,"",8436,74.7,""],
    [3709,2003,"Lothian","Other conditions/syndromes",12,"",8436,14.2,""],
    [3710,2003,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",41,"",8436,48.6,""],
    [3711,2003,"Orkney","All major congenital conditions registerable by EUROCAT",7,"",171,409.4,""],
    [3712,2003,"Orkney","Nervous system conditions",0,"",171,0,""],
    [3713,2003,"Orkney","Eye conditions",0,"",171,0,""],
    [3714,2003,"Orkney","Ear, face and neck conditions",0,"",171,0,""],
    [3716,2003,"Orkney","Respiratory conditions",0,"",171,0,""],
    [3718,2003,"Orkney","Gastro-intestinal conditions",0,"",171,0,""],
    [3719,2003,"Orkney","Abdominal wall defects",0,"",171,0,""],
    [3720,2003,"Orkney","Kidney and urinary tract conditions",0,"",171,0,""],
    [3722,2003,"Orkney","Limb conditions",0,"",171,0,""],
    [3725,2003,"Shetland","All major congenital conditions registerable by EUROCAT",8,"",248,322.6,""],
    [3726,2003,"Shetland","Nervous system conditions",0,"",248,0,""],
    [3727,2003,"Shetland","Eye conditions",0,"",248,0,""],
    [3728,2003,"Shetland","Ear, face and neck conditions",0,"",248,0,""],
    [3729,2003,"Shetland","Congenital heart diseases (CHD)",5,"",248,201.6,""],
    [3730,2003,"Shetland","Respiratory conditions",0,"",248,0,""],
    [3731,2003,"Shetland","Oro-facial clefts",0,"",248,0,""],
    [3733,2003,"Shetland","Abdominal wall defects",0,"",248,0,""],
    [3734,2003,"Shetland","Kidney and urinary tract conditions",0,"",248,0,""],
    [3739,2003,"Tayside","All major congenital conditions registerable by EUROCAT",103,"",3933,261.9,""],
    [3740,2003,"Tayside","Nervous system conditions",9,"",3933,22.9,""],
    [3742,2003,"Tayside","Ear, face and neck conditions",0,"",3933,0,""],
    [3743,2003,"Tayside","Congenital heart diseases (CHD)",20,"",3933,50.9,""],
    [3745,2003,"Tayside","Oro-facial clefts",5,"",3933,12.7,""],
    [3746,2003,"Tayside","Gastro-intestinal conditions",10,"",3933,25.4,""],
    [3748,2003,"Tayside","Kidney and urinary tract conditions",5,"",3933,12.7,""],
    [3749,2003,"Tayside","Genital conditions",6,"",3933,15.3,""],
    [3750,2003,"Tayside","Limb conditions",18,"",3933,45.8,""],
    [3752,2003,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",21,"",3933,53.4,""],
    [3753,2003,"Total","All major congenital conditions registerable by EUROCAT",1572,"",52645,298.6,""],
    [3754,2003,"Total","Nervous system conditions",172,"",52645,32.7,""],
    [3755,2003,"Total","Eye conditions",40,"",52645,7.6,""],
    [3756,2003,"Total","Ear, face and neck conditions",15,"",52645,2.8,""],
    [3757,2003,"Total","Congenital heart diseases (CHD)",344,"",52645,65.3,""],
    [3758,2003,"Total","Respiratory conditions",32,"",52645,6.1,""],
    [3759,2003,"Total","Oro-facial clefts",79,"",52645,15,""],
    [3760,2003,"Total","Gastro-intestinal conditions",128,"",52645,24.3,""],
    [3761,2003,"Total","Abdominal wall defects",29,"",52645,5.5,""],
    [3762,2003,"Total","Kidney and urinary tract conditions",138,"",52645,26.2,""],
    [3763,2003,"Total","Genital conditions",180,"",52645,34.2,""],
    [3764,2003,"Total","Limb conditions",256,"",52645,48.6,""],
    [3765,2003,"Total","Other conditions/syndromes",84,"",52645,16,""],
    [3766,2003,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",263,"",52645,50,""],
    [3769,2003,"Western Isles","Eye conditions",0,"",253,0,""],
    [3770,2003,"Western Isles","Ear, face and neck conditions",0,"",253,0,""],
    [3771,2003,"Western Isles","Congenital heart diseases (CHD)",0,"",253,0,""],
    [3772,2003,"Western Isles","Respiratory conditions",0,"",253,0,""],
    [3773,2003,"Western Isles","Oro-facial clefts",0,"",253,0,""],
    [3774,2003,"Western Isles","Gastro-intestinal conditions",0,"",253,0,""],
    [3775,2003,"Western Isles","Abdominal wall defects",0,"",253,0,""],
    [3776,2003,"Western Isles","Kidney and urinary tract conditions",0,"",253,0,""],
    [3777,2003,"Western Isles","Genital conditions",0,"",253,0,""],
    [3781,2002,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",117,"",3507,333.6,""],
    [3782,2002,"Ayrshire and Arran","Nervous system conditions",11,"",3507,31.4,""],
    [3784,2002,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3507,0,""],
    [3785,2002,"Ayrshire and Arran","Congenital heart diseases (CHD)",25,"",3507,71.3,""],
    [3786,2002,"Ayrshire and Arran","Respiratory conditions",0,"",3507,0,""],
    [3788,2002,"Ayrshire and Arran","Gastro-intestinal conditions",14,"",3507,39.9,""],
    [3790,2002,"Ayrshire and Arran","Kidney and urinary tract conditions",18,"",3507,51.3,""],
    [3791,2002,"Ayrshire and Arran","Genital conditions",14,"",3507,39.9,""],
    [3792,2002,"Ayrshire and Arran","Limb conditions",22,"",3507,62.7,""],
    [3794,2002,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",17,"",3507,48.5,""],
    [3795,2002,"Borders","All major congenital conditions registerable by EUROCAT",13,"",978,132.9,""],
    [3797,2002,"Borders","Eye conditions",0,"",978,0,""],
    [3798,2002,"Borders","Ear, face and neck conditions",0,"",978,0,""],
    [3800,2002,"Borders","Respiratory conditions",0,"",978,0,""],
    [3803,2002,"Borders","Abdominal wall defects",0,"",978,0,""],
    [3804,2002,"Borders","Kidney and urinary tract conditions",0,"",978,0,""],
    [3805,2002,"Borders","Genital conditions",0,"",978,0,""],
    [3809,2002,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",49,"",1324,370.1,""],
    [3810,2002,"Dumfries and Galloway","Nervous system conditions",6,"",1324,45.3,""],
    [3813,2002,"Dumfries and Galloway","Congenital heart diseases (CHD)",12,"",1324,90.6,""],
    [3818,2002,"Dumfries and Galloway","Kidney and urinary tract conditions",9,"",1324,68,""],
    [3820,2002,"Dumfries and Galloway","Limb conditions",5,"",1324,37.8,""],
    [3822,2002,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",10,"",1324,75.5,""],
    [3823,2002,"Fife","All major congenital conditions registerable by EUROCAT",73,"",3545,205.9,""],
    [3824,2002,"Fife","Nervous system conditions",9,"",3545,25.4,""],
    [3826,2002,"Fife","Ear, face and neck conditions",0,"",3545,0,""],
    [3827,2002,"Fife","Congenital heart diseases (CHD)",20,"",3545,56.4,""],
    [3830,2002,"Fife","Gastro-intestinal conditions",7,"",3545,19.7,""],
    [3833,2002,"Fife","Genital conditions",5,"",3545,14.1,""],
    [3834,2002,"Fife","Limb conditions",10,"",3545,28.2,""],
    [3836,2002,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",11,"",3545,31,""],
    [3837,2002,"Forth Valley","All major congenital conditions registerable by EUROCAT",82,"",2819,290.9,""],
    [3838,2002,"Forth Valley","Nervous system conditions",11,"",2819,39,""],
    [3840,2002,"Forth Valley","Ear, face and neck conditions",0,"",2819,0,""],
    [3841,2002,"Forth Valley","Congenital heart diseases (CHD)",19,"",2819,67.4,""],
    [3843,2002,"Forth Valley","Oro-facial clefts",5,"",2819,17.7,""],
    [3844,2002,"Forth Valley","Gastro-intestinal conditions",5,"",2819,17.7,""],
    [3846,2002,"Forth Valley","Kidney and urinary tract conditions",10,"",2819,35.5,""],
    [3847,2002,"Forth Valley","Genital conditions",7,"",2819,24.8,""],
    [3848,2002,"Forth Valley","Limb conditions",12,"",2819,42.6,""],
    [3850,2002,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",12,"",2819,42.6,""],
    [3851,2002,"Grampian","All major congenital conditions registerable by EUROCAT",212,"",5317,398.7,""],
    [3852,2002,"Grampian","Nervous system conditions",18,"",5317,33.9,""],
    [3855,2002,"Grampian","Congenital heart diseases (CHD)",37,"",5317,69.6,""],
    [3858,2002,"Grampian","Gastro-intestinal conditions",18,"",5317,33.9,""],
    [3860,2002,"Grampian","Kidney and urinary tract conditions",24,"",5317,45.1,""],
    [3861,2002,"Grampian","Genital conditions",22,"",5317,41.4,""],
    [3862,2002,"Grampian","Limb conditions",51,"",5317,95.9,""],
    [3863,2002,"Grampian","Other conditions/syndromes",11,"",5317,20.7,""],
    [3864,2002,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",25,"",5317,47,""],
    [3865,2002,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",261,"",11782,221.5,""],
    [3866,2002,"Greater Glasgow and Clyde","Nervous system conditions",25,"",11782,21.2,""],
    [3867,2002,"Greater Glasgow and Clyde","Eye conditions",11,"",11782,9.3,""],
    [3869,2002,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",72,"",11782,61.1,""],
    [3870,2002,"Greater Glasgow and Clyde","Respiratory conditions",9,"",11782,7.6,""],
    [3871,2002,"Greater Glasgow and Clyde","Oro-facial clefts",22,"",11782,18.7,""],
    [3872,2002,"Greater Glasgow and Clyde","Gastro-intestinal conditions",22,"",11782,18.7,""],
    [3873,2002,"Greater Glasgow and Clyde","Abdominal wall defects",8,"",11782,6.8,""],
    [3874,2002,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",19,"",11782,16.1,""],
    [3875,2002,"Greater Glasgow and Clyde","Genital conditions",25,"",11782,21.2,""],
    [3876,2002,"Greater Glasgow and Clyde","Limb conditions",24,"",11782,20.4,""],
    [3877,2002,"Greater Glasgow and Clyde","Other conditions/syndromes",17,"",11782,14.4,""],
    [3878,2002,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",44,"",11782,37.3,""],
    [3879,2002,"Highland","All major congenital conditions registerable by EUROCAT",73,"",2751,265.4,""],
    [3880,2002,"Highland","Nervous system conditions",6,"",2751,21.8,""],
    [3881,2002,"Highland","Eye conditions",0,"",2751,0,""],
    [3883,2002,"Highland","Congenital heart diseases (CHD)",25,"",2751,90.9,""],
    [3887,2002,"Highland","Abdominal wall defects",0,"",2751,0,""],
    [3888,2002,"Highland","Kidney and urinary tract conditions",9,"",2751,32.7,""],
    [3889,2002,"Highland","Genital conditions",6,"",2751,21.8,""],
    [3890,2002,"Highland","Limb conditions",17,"",2751,61.8,""],
    [3892,2002,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",12,"",2751,43.6,""],
    [3893,2002,"Lanarkshire","All major congenital conditions registerable by EUROCAT",136,"",6771,200.9,""],
    [3894,2002,"Lanarkshire","Nervous system conditions",18,"",6771,26.6,""],
    [3895,2002,"Lanarkshire","Eye conditions",0,"",6771,0,""],
    [3896,2002,"Lanarkshire","Ear, face and neck conditions",0,"",6771,0,""],
    [3897,2002,"Lanarkshire","Congenital heart diseases (CHD)",31,"",6771,45.8,""],
    [3898,2002,"Lanarkshire","Respiratory conditions",6,"",6771,8.9,""],
    [3899,2002,"Lanarkshire","Oro-facial clefts",10,"",6771,14.8,""],
    [3900,2002,"Lanarkshire","Gastro-intestinal conditions",15,"",6771,22.2,""],
    [3901,2002,"Lanarkshire","Abdominal wall defects",5,"",6771,7.4,""],
    [3902,2002,"Lanarkshire","Kidney and urinary tract conditions",14,"",6771,20.7,""],
    [3903,2002,"Lanarkshire","Genital conditions",10,"",6771,14.8,""],
    [3904,2002,"Lanarkshire","Limb conditions",13,"",6771,19.2,""],
    [3905,2002,"Lanarkshire","Other conditions/syndromes",7,"",6771,10.3,""],
    [3906,2002,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",22,"",6771,32.5,""],
    [3907,2002,"Lothian","All major congenital conditions registerable by EUROCAT",227,"",8178,277.6,""],
    [3908,2002,"Lothian","Nervous system conditions",22,"",8178,26.9,""],
    [3909,2002,"Lothian","Eye conditions",7,"",8178,8.6,""],
    [3910,2002,"Lothian","Ear, face and neck conditions",5,"",8178,6.1,""],
    [3911,2002,"Lothian","Congenital heart diseases (CHD)",31,"",8178,37.9,""],
    [3913,2002,"Lothian","Oro-facial clefts",6,"",8178,7.3,""],
    [3914,2002,"Lothian","Gastro-intestinal conditions",20,"",8178,24.5,""],
    [3916,2002,"Lothian","Kidney and urinary tract conditions",17,"",8178,20.8,""],
    [3917,2002,"Lothian","Genital conditions",28,"",8178,34.2,""],
    [3918,2002,"Lothian","Limb conditions",49,"",8178,59.9,""],
    [3919,2002,"Lothian","Other conditions/syndromes",10,"",8178,12.2,""],
    [3920,2002,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",38,"",8178,46.5,""],
    [3921,2002,"Orkney","All major congenital conditions registerable by EUROCAT",5,"",165,303,""],
    [3923,2002,"Orkney","Eye conditions",0,"",165,0,""],
    [3924,2002,"Orkney","Ear, face and neck conditions",0,"",165,0,""],
    [3925,2002,"Orkney","Congenital heart diseases (CHD)",0,"",165,0,""],
    [3926,2002,"Orkney","Respiratory conditions",0,"",165,0,""],
    [3927,2002,"Orkney","Oro-facial clefts",0,"",165,0,""],
    [3928,2002,"Orkney","Gastro-intestinal conditions",0,"",165,0,""],
    [3929,2002,"Orkney","Abdominal wall defects",0,"",165,0,""],
    [3930,2002,"Orkney","Kidney and urinary tract conditions",0,"",165,0,""],
    [3931,2002,"Orkney","Genital conditions",0,"",165,0,""],
    [3933,2002,"Orkney","Other conditions/syndromes",0,"",165,0,""],
    [3935,2002,"Shetland","All major congenital conditions registerable by EUROCAT",6,"",216,277.8,""],
    [3937,2002,"Shetland","Eye conditions",0,"",216,0,""],
    [3938,2002,"Shetland","Ear, face and neck conditions",0,"",216,0,""],
    [3940,2002,"Shetland","Respiratory conditions",0,"",216,0,""],
    [3941,2002,"Shetland","Oro-facial clefts",0,"",216,0,""],
    [3942,2002,"Shetland","Gastro-intestinal conditions",0,"",216,0,""],
    [3943,2002,"Shetland","Abdominal wall defects",0,"",216,0,""],
    [3944,2002,"Shetland","Kidney and urinary tract conditions",0,"",216,0,""],
    [3945,2002,"Shetland","Genital conditions",0,"",216,0,""],
    [3947,2002,"Shetland","Other conditions/syndromes",0,"",216,0,""],
    [3949,2002,"Tayside","All major congenital conditions registerable by EUROCAT",82,"",3693,222,""],
    [3950,2002,"Tayside","Nervous system conditions",7,"",3693,19,""],
    [3952,2002,"Tayside","Ear, face and neck conditions",0,"",3693,0,""],
    [3953,2002,"Tayside","Congenital heart diseases (CHD)",15,"",3693,40.6,""],
    [3954,2002,"Tayside","Respiratory conditions",0,"",3693,0,""],
    [3955,2002,"Tayside","Oro-facial clefts",6,"",3693,16.2,""],
    [3956,2002,"Tayside","Gastro-intestinal conditions",9,"",3693,24.4,""],
    [3958,2002,"Tayside","Kidney and urinary tract conditions",5,"",3693,13.5,""],
    [3960,2002,"Tayside","Limb conditions",15,"",3693,40.6,""],
    [3962,2002,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",16,"",3693,43.3,""],
    [3963,2002,"Total","All major congenital conditions registerable by EUROCAT",1344,"",51520,260.9,""],
    [3964,2002,"Total","Nervous system conditions",138,"",51520,26.8,""],
    [3965,2002,"Total","Eye conditions",33,"",51520,6.4,""],
    [3966,2002,"Total","Ear, face and neck conditions",11,"",51520,2.1,""],
    [3967,2002,"Total","Congenital heart diseases (CHD)",293,"",51520,56.9,""],
    [3968,2002,"Total","Respiratory conditions",29,"",51520,5.6,""],
    [3969,2002,"Total","Oro-facial clefts",70,"",51520,13.6,""],
    [3970,2002,"Total","Gastro-intestinal conditions",117,"",51520,22.7,""],
    [3971,2002,"Total","Abdominal wall defects",26,"",51520,5,""],
    [3972,2002,"Total","Kidney and urinary tract conditions",130,"",51520,25.2,""],
    [3973,2002,"Total","Genital conditions",124,"",51520,24.1,""],
    [3974,2002,"Total","Limb conditions",226,"",51520,43.9,""],
    [3975,2002,"Total","Other conditions/syndromes",63,"",51520,12.2,""],
    [3976,2002,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",215,"",51520,41.7,""],
    [3979,2002,"Western Isles","Eye conditions",0,"",242,0,""],
    [3980,2002,"Western Isles","Ear, face and neck conditions",0,"",242,0,""],
    [3981,2002,"Western Isles","Congenital heart diseases (CHD)",0,"",242,0,""],
    [3982,2002,"Western Isles","Respiratory conditions",0,"",242,0,""],
    [3983,2002,"Western Isles","Oro-facial clefts",0,"",242,0,""],
    [3984,2002,"Western Isles","Gastro-intestinal conditions",0,"",242,0,""],
    [3985,2002,"Western Isles","Abdominal wall defects",0,"",242,0,""],
    [3987,2002,"Western Isles","Genital conditions",0,"",242,0,""],
    [3989,2002,"Western Isles","Other conditions/syndromes",0,"",242,0,""],
    [3991,2001,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",98,"",3660,267.8,""],
    [3992,2001,"Ayrshire and Arran","Nervous system conditions",8,"",3660,21.9,""],
    [3993,2001,"Ayrshire and Arran","Eye conditions",0,"",3660,0,""],
    [3994,2001,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3660,0,""],
    [3995,2001,"Ayrshire and Arran","Congenital heart diseases (CHD)",25,"",3660,68.3,""],
    [4000,2001,"Ayrshire and Arran","Kidney and urinary tract conditions",8,"",3660,21.9,""],
    [4001,2001,"Ayrshire and Arran","Genital conditions",9,"",3660,24.6,""],
    [4002,2001,"Ayrshire and Arran","Limb conditions",17,"",3660,46.4,""],
    [4003,2001,"Ayrshire and Arran","Other conditions/syndromes",6,"",3660,16.4,""],
    [4004,2001,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",22,"",3660,60.1,""],
    [4005,2001,"Borders","All major congenital conditions registerable by EUROCAT",16,"",1018,157.2,""],
    [4007,2001,"Borders","Eye conditions",0,"",1018,0,""],
    [4008,2001,"Borders","Ear, face and neck conditions",0,"",1018,0,""],
    [4009,2001,"Borders","Congenital heart diseases (CHD)",6,"",1018,58.9,""],
    [4010,2001,"Borders","Respiratory conditions",0,"",1018,0,""],
    [4012,2001,"Borders","Gastro-intestinal conditions",0,"",1018,0,""],
    [4013,2001,"Borders","Abdominal wall defects",0,"",1018,0,""],
    [4015,2001,"Borders","Genital conditions",0,"",1018,0,""],
    [4019,2001,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",46,"",1270,362.2,""],
    [4022,2001,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1270,0,""],
    [4023,2001,"Dumfries and Galloway","Congenital heart diseases (CHD)",7,"",1270,55.1,""],
    [4025,2001,"Dumfries and Galloway","Oro-facial clefts",0,"",1270,0,""],
    [4027,2001,"Dumfries and Galloway","Abdominal wall defects",0,"",1270,0,""],
    [4028,2001,"Dumfries and Galloway","Kidney and urinary tract conditions",13,"",1270,102.4,""],
    [4029,2001,"Dumfries and Galloway","Genital conditions",9,"",1270,70.9,""],
    [4030,2001,"Dumfries and Galloway","Limb conditions",6,"",1270,47.2,""],
    [4032,2001,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",9,"",1270,70.9,""],
    [4033,2001,"Fife","All major congenital conditions registerable by EUROCAT",80,"",3650,219.2,""],
    [4034,2001,"Fife","Nervous system conditions",12,"",3650,32.9,""],
    [4037,2001,"Fife","Congenital heart diseases (CHD)",15,"",3650,41.1,""],
    [4039,2001,"Fife","Oro-facial clefts",8,"",3650,21.9,""],
    [4040,2001,"Fife","Gastro-intestinal conditions",9,"",3650,24.7,""],
    [4043,2001,"Fife","Genital conditions",8,"",3650,21.9,""],
    [4044,2001,"Fife","Limb conditions",12,"",3650,32.9,""],
    [4046,2001,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",13,"",3650,35.6,""],
    [4047,2001,"Forth Valley","All major congenital conditions registerable by EUROCAT",97,"",2809,345.3,""],
    [4048,2001,"Forth Valley","Nervous system conditions",12,"",2809,42.7,""],
    [4050,2001,"Forth Valley","Ear, face and neck conditions",0,"",2809,0,""],
    [4051,2001,"Forth Valley","Congenital heart diseases (CHD)",18,"",2809,64.1,""],
    [4054,2001,"Forth Valley","Gastro-intestinal conditions",8,"",2809,28.5,""],
    [4056,2001,"Forth Valley","Kidney and urinary tract conditions",9,"",2809,32,""],
    [4057,2001,"Forth Valley","Genital conditions",9,"",2809,32,""],
    [4058,2001,"Forth Valley","Limb conditions",18,"",2809,64.1,""],
    [4060,2001,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",19,"",2809,67.6,""],
    [4061,2001,"Grampian","All major congenital conditions registerable by EUROCAT",207,"",5201,398,""],
    [4062,2001,"Grampian","Nervous system conditions",15,"",5201,28.8,""],
    [4063,2001,"Grampian","Eye conditions",5,"",5201,9.6,""],
    [4065,2001,"Grampian","Congenital heart diseases (CHD)",44,"",5201,84.6,""],
    [4066,2001,"Grampian","Respiratory conditions",5,"",5201,9.6,""],
    [4067,2001,"Grampian","Oro-facial clefts",7,"",5201,13.5,""],
    [4068,2001,"Grampian","Gastro-intestinal conditions",28,"",5201,53.8,""],
    [4069,2001,"Grampian","Abdominal wall defects",0,"",5201,0,""],
    [4070,2001,"Grampian","Kidney and urinary tract conditions",18,"",5201,34.6,""],
    [4071,2001,"Grampian","Genital conditions",21,"",5201,40.4,""],
    [4072,2001,"Grampian","Limb conditions",40,"",5201,76.9,""],
    [4073,2001,"Grampian","Other conditions/syndromes",15,"",5201,28.8,""],
    [4074,2001,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",37,"",5201,71.1,""],
    [4075,2001,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",325,"",12116,268.2,""],
    [4076,2001,"Greater Glasgow and Clyde","Nervous system conditions",22,"",12116,18.2,""],
    [4077,2001,"Greater Glasgow and Clyde","Eye conditions",7,"",12116,5.8,""],
    [4079,2001,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",68,"",12116,56.1,""],
    [4080,2001,"Greater Glasgow and Clyde","Respiratory conditions",15,"",12116,12.4,""],
    [4081,2001,"Greater Glasgow and Clyde","Oro-facial clefts",23,"",12116,19,""],
    [4082,2001,"Greater Glasgow and Clyde","Gastro-intestinal conditions",31,"",12116,25.6,""],
    [4083,2001,"Greater Glasgow and Clyde","Abdominal wall defects",5,"",12116,4.1,""],
    [4084,2001,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",22,"",12116,18.2,""],
    [4085,2001,"Greater Glasgow and Clyde","Genital conditions",34,"",12116,28.1,""],
    [4086,2001,"Greater Glasgow and Clyde","Limb conditions",48,"",12116,39.6,""],
    [4087,2001,"Greater Glasgow and Clyde","Other conditions/syndromes",20,"",12116,16.5,""],
    [4088,2001,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",60,"",12116,49.5,""],
    [4089,2001,"Highland","All major congenital conditions registerable by EUROCAT",73,"",2891,252.5,""],
    [4090,2001,"Highland","Nervous system conditions",10,"",2891,34.6,""],
    [4093,2001,"Highland","Congenital heart diseases (CHD)",19,"",2891,65.7,""],
    [4096,2001,"Highland","Gastro-intestinal conditions",6,"",2891,20.8,""],
    [4099,2001,"Highland","Genital conditions",6,"",2891,20.8,""],
    [4100,2001,"Highland","Limb conditions",23,"",2891,79.6,""],
    [4102,2001,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",9,"",2891,31.1,""],
    [4103,2001,"Lanarkshire","All major congenital conditions registerable by EUROCAT",138,"",6830,202,""],
    [4104,2001,"Lanarkshire","Nervous system conditions",19,"",6830,27.8,""],
    [4106,2001,"Lanarkshire","Ear, face and neck conditions",0,"",6830,0,""],
    [4107,2001,"Lanarkshire","Congenital heart diseases (CHD)",37,"",6830,54.2,""],
    [4108,2001,"Lanarkshire","Respiratory conditions",6,"",6830,8.8,""],
    [4110,2001,"Lanarkshire","Gastro-intestinal conditions",17,"",6830,24.9,""],
    [4111,2001,"Lanarkshire","Abdominal wall defects",6,"",6830,8.8,""],
    [4112,2001,"Lanarkshire","Kidney and urinary tract conditions",13,"",6830,19,""],
    [4113,2001,"Lanarkshire","Genital conditions",6,"",6830,8.8,""],
    [4114,2001,"Lanarkshire","Limb conditions",21,"",6830,30.7,""],
    [4115,2001,"Lanarkshire","Other conditions/syndromes",11,"",6830,16.1,""],
    [4116,2001,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",21,"",6830,30.7,""],
    [4117,2001,"Lothian","All major congenital conditions registerable by EUROCAT",280,"",8348,335.4,""],
    [4118,2001,"Lothian","Nervous system conditions",18,"",8348,21.6,""],
    [4119,2001,"Lothian","Eye conditions",5,"",8348,6,""],
    [4120,2001,"Lothian","Ear, face and neck conditions",5,"",8348,6,""],
    [4121,2001,"Lothian","Congenital heart diseases (CHD)",55,"",8348,65.9,""],
    [4122,2001,"Lothian","Respiratory conditions",6,"",8348,7.2,""],
    [4123,2001,"Lothian","Oro-facial clefts",9,"",8348,10.8,""],
    [4124,2001,"Lothian","Gastro-intestinal conditions",27,"",8348,32.3,""],
    [4126,2001,"Lothian","Kidney and urinary tract conditions",20,"",8348,24,""],
    [4127,2001,"Lothian","Genital conditions",52,"",8348,62.3,""],
    [4128,2001,"Lothian","Limb conditions",55,"",8348,65.9,""],
    [4129,2001,"Lothian","Other conditions/syndromes",9,"",8348,10.8,""],
    [4130,2001,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",43,"",8348,51.5,""],
    [4133,2001,"Orkney","Eye conditions",0,"",176,0,""],
    [4134,2001,"Orkney","Ear, face and neck conditions",0,"",176,0,""],
    [4136,2001,"Orkney","Respiratory conditions",0,"",176,0,""],
    [4137,2001,"Orkney","Oro-facial clefts",0,"",176,0,""],
    [4138,2001,"Orkney","Gastro-intestinal conditions",0,"",176,0,""],
    [4139,2001,"Orkney","Abdominal wall defects",0,"",176,0,""],
    [4140,2001,"Orkney","Kidney and urinary tract conditions",0,"",176,0,""],
    [4141,2001,"Orkney","Genital conditions",0,"",176,0,""],
    [4142,2001,"Orkney","Limb conditions",0,"",176,0,""],
    [4143,2001,"Orkney","Other conditions/syndromes",0,"",176,0,""],
    [4145,2001,"Shetland","All major congenital conditions registerable by EUROCAT",11,"",238,462.2,""],
    [4148,2001,"Shetland","Ear, face and neck conditions",0,"",238,0,""],
    [4151,2001,"Shetland","Oro-facial clefts",0,"",238,0,""],
    [4154,2001,"Shetland","Kidney and urinary tract conditions",0,"",238,0,""],
    [4156,2001,"Shetland","Limb conditions",0,"",238,0,""],
    [4159,2001,"Tayside","All major congenital conditions registerable by EUROCAT",82,"",3908,209.8,""],
    [4160,2001,"Tayside","Nervous system conditions",10,"",3908,25.6,""],
    [4161,2001,"Tayside","Eye conditions",0,"",3908,0,""],
    [4162,2001,"Tayside","Ear, face and neck conditions",0,"",3908,0,""],
    [4163,2001,"Tayside","Congenital heart diseases (CHD)",20,"",3908,51.2,""],
    [4164,2001,"Tayside","Respiratory conditions",5,"",3908,12.8,""],
    [4165,2001,"Tayside","Oro-facial clefts",6,"",3908,15.4,""],
    [4168,2001,"Tayside","Kidney and urinary tract conditions",8,"",3908,20.5,""],
    [4170,2001,"Tayside","Limb conditions",8,"",3908,20.5,""],
    [4172,2001,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",22,"",3908,56.3,""],
    [4173,2001,"Total","All major congenital conditions registerable by EUROCAT",1468,"",52573,279.2,""],
    [4174,2001,"Total","Nervous system conditions",136,"",52573,25.9,""],
    [4175,2001,"Total","Eye conditions",26,"",52573,4.9,""],
    [4176,2001,"Total","Ear, face and neck conditions",11,"",52573,2.1,""],
    [4177,2001,"Total","Congenital heart diseases (CHD)",319,"",52573,60.7,""],
    [4178,2001,"Total","Respiratory conditions",50,"",52573,9.5,""],
    [4179,2001,"Total","Oro-facial clefts",69,"",52573,13.1,""],
    [4180,2001,"Total","Gastro-intestinal conditions",145,"",52573,27.6,""],
    [4181,2001,"Total","Abdominal wall defects",29,"",52573,5.5,""],
    [4182,2001,"Total","Kidney and urinary tract conditions",115,"",52573,21.9,""],
    [4183,2001,"Total","Genital conditions",160,"",52573,30.4,""],
    [4184,2001,"Total","Limb conditions",255,"",52573,48.5,""],
    [4185,2001,"Total","Other conditions/syndromes",79,"",52573,15,""],
    [4186,2001,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",263,"",52573,50,""],
    [4188,2001,"Western Isles","Nervous system conditions",0,"",227,0,""],
    [4189,2001,"Western Isles","Eye conditions",0,"",227,0,""],
    [4190,2001,"Western Isles","Ear, face and neck conditions",0,"",227,0,""],
    [4191,2001,"Western Isles","Congenital heart diseases (CHD)",0,"",227,0,""],
    [4192,2001,"Western Isles","Respiratory conditions",0,"",227,0,""],
    [4193,2001,"Western Isles","Oro-facial clefts",0,"",227,0,""],
    [4195,2001,"Western Isles","Abdominal wall defects",0,"",227,0,""],
    [4196,2001,"Western Isles","Kidney and urinary tract conditions",0,"",227,0,""],
    [4197,2001,"Western Isles","Genital conditions",0,"",227,0,""],
    [4198,2001,"Western Isles","Limb conditions",0,"",227,0,""],
    [4199,2001,"Western Isles","Other conditions/syndromes",0,"",227,0,""],
    [4201,2000,"Ayrshire and Arran","All major congenital conditions registerable by EUROCAT",154,"",3677,418.8,""],
    [4202,2000,"Ayrshire and Arran","Nervous system conditions",12,"",3677,32.6,""],
    [4204,2000,"Ayrshire and Arran","Ear, face and neck conditions",0,"",3677,0,""],
    [4205,2000,"Ayrshire and Arran","Congenital heart diseases (CHD)",25,"",3677,68,""],
    [4207,2000,"Ayrshire and Arran","Oro-facial clefts",5,"",3677,13.6,""],
    [4208,2000,"Ayrshire and Arran","Gastro-intestinal conditions",5,"",3677,13.6,""],
    [4209,2000,"Ayrshire and Arran","Abdominal wall defects",6,"",3677,16.3,""],
    [4210,2000,"Ayrshire and Arran","Kidney and urinary tract conditions",18,"",3677,49,""],
    [4211,2000,"Ayrshire and Arran","Genital conditions",11,"",3677,29.9,""],
    [4212,2000,"Ayrshire and Arran","Limb conditions",71,"",3677,193.1,""],
    [4213,2000,"Ayrshire and Arran","Other conditions/syndromes",6,"",3677,16.3,""],
    [4214,2000,"Ayrshire and Arran","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",13,"",3677,35.4,""],
    [4215,2000,"Borders","All major congenital conditions registerable by EUROCAT",19,"",1022,185.9,""],
    [4218,2000,"Borders","Ear, face and neck conditions",0,"",1022,0,""],
    [4220,2000,"Borders","Respiratory conditions",0,"",1022,0,""],
    [4221,2000,"Borders","Oro-facial clefts",0,"",1022,0,""],
    [4223,2000,"Borders","Abdominal wall defects",0,"",1022,0,""],
    [4227,2000,"Borders","Other conditions/syndromes",0,"",1022,0,""],
    [4229,2000,"Dumfries and Galloway","All major congenital conditions registerable by EUROCAT",31,"",1369,226.4,""],
    [4230,2000,"Dumfries and Galloway","Nervous system conditions",5,"",1369,36.5,""],
    [4231,2000,"Dumfries and Galloway","Eye conditions",0,"",1369,0,""],
    [4232,2000,"Dumfries and Galloway","Ear, face and neck conditions",0,"",1369,0,""],
    [4233,2000,"Dumfries and Galloway","Congenital heart diseases (CHD)",7,"",1369,51.1,""],
    [4237,2000,"Dumfries and Galloway","Abdominal wall defects",0,"",1369,0,""],
    [4241,2000,"Dumfries and Galloway","Other conditions/syndromes",0,"",1369,0,""],
    [4242,2000,"Dumfries and Galloway","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",7,"",1369,51.1,""],
    [4243,2000,"Fife","All major congenital conditions registerable by EUROCAT",92,"",3528,260.8,""],
    [4244,2000,"Fife","Nervous system conditions",14,"",3528,39.7,""],
    [4246,2000,"Fife","Ear, face and neck conditions",0,"",3528,0,""],
    [4247,2000,"Fife","Congenital heart diseases (CHD)",20,"",3528,56.7,""],
    [4249,2000,"Fife","Oro-facial clefts",8,"",3528,22.7,""],
    [4254,2000,"Fife","Limb conditions",9,"",3528,25.5,""],
    [4256,2000,"Fife","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",26,"",3528,73.7,""],
    [4257,2000,"Forth Valley","All major congenital conditions registerable by EUROCAT",90,"",2952,304.9,""],
    [4258,2000,"Forth Valley","Nervous system conditions",9,"",2952,30.5,""],
    [4260,2000,"Forth Valley","Ear, face and neck conditions",0,"",2952,0,""],
    [4261,2000,"Forth Valley","Congenital heart diseases (CHD)",27,"",2952,91.5,""],
    [4262,2000,"Forth Valley","Respiratory conditions",6,"",2952,20.3,""],
    [4264,2000,"Forth Valley","Gastro-intestinal conditions",8,"",2952,27.1,""],
    [4265,2000,"Forth Valley","Abdominal wall defects",0,"",2952,0,""],
    [4267,2000,"Forth Valley","Genital conditions",10,"",2952,33.9,""],
    [4268,2000,"Forth Valley","Limb conditions",13,"",2952,44,""],
    [4270,2000,"Forth Valley","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",2952,50.8,""],
    [4271,2000,"Grampian","All major congenital conditions registerable by EUROCAT",205,"",5386,380.6,""],
    [4272,2000,"Grampian","Nervous system conditions",16,"",5386,29.7,""],
    [4273,2000,"Grampian","Eye conditions",5,"",5386,9.3,""],
    [4275,2000,"Grampian","Congenital heart diseases (CHD)",48,"",5386,89.1,""],
    [4277,2000,"Grampian","Oro-facial clefts",8,"",5386,14.9,""],
    [4278,2000,"Grampian","Gastro-intestinal conditions",13,"",5386,24.1,""],
    [4280,2000,"Grampian","Kidney and urinary tract conditions",17,"",5386,31.6,""],
    [4281,2000,"Grampian","Genital conditions",20,"",5386,37.1,""],
    [4282,2000,"Grampian","Limb conditions",45,"",5386,83.5,""],
    [4283,2000,"Grampian","Other conditions/syndromes",11,"",5386,20.4,""],
    [4284,2000,"Grampian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",28,"",5386,52,""],
    [4285,2000,"Greater Glasgow and Clyde","All major congenital conditions registerable by EUROCAT",343,"",12500,274.4,""],
    [4286,2000,"Greater Glasgow and Clyde","Nervous system conditions",36,"",12500,28.8,""],
    [4287,2000,"Greater Glasgow and Clyde","Eye conditions",6,"",12500,4.8,""],
    [4289,2000,"Greater Glasgow and Clyde","Congenital heart diseases (CHD)",79,"",12500,63.2,""],
    [4290,2000,"Greater Glasgow and Clyde","Respiratory conditions",19,"",12500,15.2,""],
    [4291,2000,"Greater Glasgow and Clyde","Oro-facial clefts",21,"",12500,16.8,""],
    [4292,2000,"Greater Glasgow and Clyde","Gastro-intestinal conditions",35,"",12500,28,""],
    [4293,2000,"Greater Glasgow and Clyde","Abdominal wall defects",6,"",12500,4.8,""],
    [4294,2000,"Greater Glasgow and Clyde","Kidney and urinary tract conditions",30,"",12500,24,""],
    [4295,2000,"Greater Glasgow and Clyde","Genital conditions",27,"",12500,21.6,""],
    [4296,2000,"Greater Glasgow and Clyde","Limb conditions",52,"",12500,41.6,""],
    [4297,2000,"Greater Glasgow and Clyde","Other conditions/syndromes",13,"",12500,10.4,""],
    [4298,2000,"Greater Glasgow and Clyde","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",63,"",12500,50.4,""],
    [4299,2000,"Highland","All major congenital conditions registerable by EUROCAT",103,"",2976,346.1,""],
    [4300,2000,"Highland","Nervous system conditions",9,"",2976,30.2,""],
    [4303,2000,"Highland","Congenital heart diseases (CHD)",16,"",2976,53.8,""],
    [4306,2000,"Highland","Gastro-intestinal conditions",5,"",2976,16.8,""],
    [4308,2000,"Highland","Kidney and urinary tract conditions",11,"",2976,37,""],
    [4309,2000,"Highland","Genital conditions",12,"",2976,40.3,""],
    [4310,2000,"Highland","Limb conditions",26,"",2976,87.4,""],
    [4312,2000,"Highland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",15,"",2976,50.4,""],
    [4313,2000,"Lanarkshire","All major congenital conditions registerable by EUROCAT",142,"",7037,201.8,""],
    [4314,2000,"Lanarkshire","Nervous system conditions",16,"",7037,22.7,""],
    [4316,2000,"Lanarkshire","Ear, face and neck conditions",0,"",7037,0,""],
    [4317,2000,"Lanarkshire","Congenital heart diseases (CHD)",29,"",7037,41.2,""],
    [4319,2000,"Lanarkshire","Oro-facial clefts",9,"",7037,12.8,""],
    [4320,2000,"Lanarkshire","Gastro-intestinal conditions",13,"",7037,18.5,""],
    [4321,2000,"Lanarkshire","Abdominal wall defects",6,"",7037,8.5,""],
    [4322,2000,"Lanarkshire","Kidney and urinary tract conditions",9,"",7037,12.8,""],
    [4323,2000,"Lanarkshire","Genital conditions",16,"",7037,22.7,""],
    [4324,2000,"Lanarkshire","Limb conditions",27,"",7037,38.4,""],
    [4325,2000,"Lanarkshire","Other conditions/syndromes",8,"",7037,11.4,""],
    [4326,2000,"Lanarkshire","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",26,"",7037,36.9,""],
    [4327,2000,"Lothian","All major congenital conditions registerable by EUROCAT",315,"",8501,370.5,""],
    [4328,2000,"Lothian","Nervous system conditions",27,"",8501,31.8,""],
    [4331,2000,"Lothian","Congenital heart diseases (CHD)",39,"",8501,45.9,""],
    [4332,2000,"Lothian","Respiratory conditions",9,"",8501,10.6,""],
    [4333,2000,"Lothian","Oro-facial clefts",8,"",8501,9.4,""],
    [4334,2000,"Lothian","Gastro-intestinal conditions",26,"",8501,30.6,""],
    [4336,2000,"Lothian","Kidney and urinary tract conditions",19,"",8501,22.4,""],
    [4337,2000,"Lothian","Genital conditions",43,"",8501,50.6,""],
    [4338,2000,"Lothian","Limb conditions",77,"",8501,90.6,""],
    [4339,2000,"Lothian","Other conditions/syndromes",15,"",8501,17.6,""],
    [4340,2000,"Lothian","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",37,"",8501,43.5,""],
    [4341,2000,"Orkney","All major congenital conditions registerable by EUROCAT",5,"",156,320.5,""],
    [4343,2000,"Orkney","Eye conditions",0,"",156,0,""],
    [4344,2000,"Orkney","Ear, face and neck conditions",0,"",156,0,""],
    [4346,2000,"Orkney","Respiratory conditions",0,"",156,0,""],
    [4347,2000,"Orkney","Oro-facial clefts",0,"",156,0,""],
    [4349,2000,"Orkney","Abdominal wall defects",0,"",156,0,""],
    [4353,2000,"Orkney","Other conditions/syndromes",0,"",156,0,""],
    [4355,2000,"Shetland","All major congenital conditions registerable by EUROCAT",6,"",235,255.3,""],
    [4356,2000,"Shetland","Nervous system conditions",0,"",235,0,""],
    [4357,2000,"Shetland","Eye conditions",0,"",235,0,""],
    [4358,2000,"Shetland","Ear, face and neck conditions",0,"",235,0,""],
    [4360,2000,"Shetland","Respiratory conditions",0,"",235,0,""],
    [4361,2000,"Shetland","Oro-facial clefts",0,"",235,0,""],
    [4363,2000,"Shetland","Abdominal wall defects",0,"",235,0,""],
    [4364,2000,"Shetland","Kidney and urinary tract conditions",0,"",235,0,""],
    [4365,2000,"Shetland","Genital conditions",0,"",235,0,""],
    [4367,2000,"Shetland","Other conditions/syndromes",0,"",235,0,""],
    [4368,2000,"Shetland","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",235,0,""],
    [4369,2000,"Tayside","All major congenital conditions registerable by EUROCAT",88,"",3852,228.5,""],
    [4370,2000,"Tayside","Nervous system conditions",13,"",3852,33.7,""],
    [4372,2000,"Tayside","Ear, face and neck conditions",0,"",3852,0,""],
    [4373,2000,"Tayside","Congenital heart diseases (CHD)",16,"",3852,41.5,""],
    [4376,2000,"Tayside","Gastro-intestinal conditions",10,"",3852,26,""],
    [4377,2000,"Tayside","Abdominal wall defects",6,"",3852,15.6,""],
    [4378,2000,"Tayside","Kidney and urinary tract conditions",5,"",3852,13,""],
    [4379,2000,"Tayside","Genital conditions",9,"",3852,23.4,""],
    [4380,2000,"Tayside","Limb conditions",16,"",3852,41.5,""],
    [4381,2000,"Tayside","Other conditions/syndromes",5,"",3852,13,""],
    [4382,2000,"Tayside","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",13,"",3852,33.7,""],
    [4383,2000,"Total","All major congenital conditions registerable by EUROCAT",1604,"",53644,299,""],
    [4384,2000,"Total","Nervous system conditions",163,"",53644,30.4,""],
    [4385,2000,"Total","Eye conditions",29,"",53644,5.4,""],
    [4386,2000,"Total","Ear, face and neck conditions",7,"",53644,1.3,""],
    [4387,2000,"Total","Congenital heart diseases (CHD)",316,"",53644,58.9,""],
    [4388,2000,"Total","Respiratory conditions",49,"",53644,9.1,""],
    [4389,2000,"Total","Oro-facial clefts",73,"",53644,13.6,""],
    [4390,2000,"Total","Gastro-intestinal conditions",126,"",53644,23.5,""],
    [4391,2000,"Total","Abdominal wall defects",36,"",53644,6.7,""],
    [4392,2000,"Total","Kidney and urinary tract conditions",125,"",53644,23.3,""],
    [4393,2000,"Total","Genital conditions",156,"",53644,29.1,""],
    [4394,2000,"Total","Limb conditions",347,"",53644,64.7,""],
    [4395,2000,"Total","Other conditions/syndromes",67,"",53644,12.5,""],
    [4396,2000,"Total","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",250,"",53644,46.6,""],
    [4397,2000,"Western Isles","All major congenital conditions registerable by EUROCAT",5,"",232,215.5,""],
    [4399,2000,"Western Isles","Eye conditions",0,"",232,0,""],
    [4400,2000,"Western Isles","Ear, face and neck conditions",0,"",232,0,""],
    [4402,2000,"Western Isles","Respiratory conditions",0,"",232,0,""],
    [4404,2000,"Western Isles","Gastro-intestinal conditions",0,"",232,0,""],
    [4405,2000,"Western Isles","Abdominal wall defects",0,"",232,0,""],
    [4406,2000,"Western Isles","Kidney and urinary tract conditions",0,"",232,0,""],
    [4407,2000,"Western Isles","Genital conditions",0,"",232,0,""],
    [4409,2000,"Western Isles","Other conditions/syndromes",0,"",232,0,""],
    [4410,2000,"Western Isles","Genetic conditions (genetic syndromes, congenital skin conditions, skeletal dysplasias, and chromosomal conditions)",0,"",232,0,""]
]}