| Column |
Type |
Label |
Description |
| BirthYear |
text |
Calender year of live birth |
|
| NumOfResult |
numeric |
Number of babies with a screening result available |
|
| NumWithNoCondition |
numeric |
Number with no condition suspected |
|
| NumWithCondition |
numeric |
Number with at least one condition suspected |
|
| NumWithCF |
numeric |
Number with cystic fibrosis suspected |
|
| NumWithSCD |
numeric |
Number with sickle cell disease (or another significant haemoglobinopathy) suspected |
|
| NumWithCHT |
numeric |
Number with primary congenital hypothyroidism suspected |
|
| NumWithPKU |
numeric |
Number with phenylketonuria suspected |
|
| NumWithMCADD |
numeric |
Number with medium-chain acyl-CoA dehydrogenase deficiency suspected |
|
| NumWithMSUD |
numeric |
Number with maple syrup urine disease suspected |
|
| NumWithHCU |
numeric |
Number with pyridoxine unresponsive homocystinuria suspected |
|
| NumWithIVA |
numeric |
Number with isovaleric acidaemia suspected |
|
| NumWithGA1 |
numeric |
Number with glutaric aciduria type 1 suspected |
|
| RatePer10000NoCondition |
numeric |
No condition suspected: rate per 10,000 screened babies |
|
| RatePer10000Condition |
numeric |
At least one condition suspected: rate per 10,000 screened babies |
|
| RatePer10000CF |
numeric |
Cystic fibrosis suspected: rate per 10,000 screened babies |
|
| RatePer10000SCD |
numeric |
Sickle cell disease (or another significant haemoglobinopathy) suspected: rate per 10,000 screened babies |
|
| RatePer10000CHT |
numeric |
Primary congenital hypothyroidism suspected: rate per 10,000 screened babies |
|
| RatePer10000PKU |
numeric |
Phenylketonuria suspected: rate per 10,000 screened babies |
|
| RatePer10000MCADD |
numeric |
Medium-chain acyl-CoA dehydrogenase deficiency suspected: rate per 10,000 screened babies |
|
| RatePer10000MSUD |
numeric |
Maple syrup urine disease suspected: rate per 10,000 screened babies |
|
| RatePer10000HCU |
numeric |
Pyridoxine unresponsive homocystinuria suspected: rate per 10,000 screened babies |
|
| RatePer10000IVA |
numeric |
Isovaleric acidaemia suspected: rate per 10,000 screened babies |
|
| RatePer10000GA1 |
numeric |
Glutaric aciduria type 1 suspected: rate per 10,000 screened babies |
|
| NumWithCarrierCF |
numeric |
Number with carrier state for cystic fibrosis suspected |
|
| NumWithCarrierSCD |
numeric |
Number with carrier state for sickle cell disease (or another significant haemoglobin variant) suspected |
|
