NewbornBloodSpotScreeningTestProceduresSnCT
| Code SystemId: | 2.16.840.1.113883.2.1.3.2.4.15 |
|---|---|
| Version: | 1.0 |
| Status: | active |
| Date: | 2014-12-18 |
Description
A subset of the SNOMED CT clinical terminology (i.e. coding system) intended for use in the UK, previously named SnomedCTUK, that describes newborn blood spot screening test procedures.
Any code from the SNOMED CT UK newborn blood spot screening test procedures subset with subset original id 61111000000134.
NB: This subset ID, 61111000000134, has not yet been defined in a release of SNOMED CT.
Values
| Code | Description | Note |
|---|---|---|
| 314081000 | Phenylketonuria screening test |
|
| 314090007 | Sickle cell disease screening test |
|
| 314080004 | Cystic fibrosis screening test |
|
| 400984005 | Congenital hypothyroidism screening test |
|
| 428056008 | Medium-chain acyl-coenzyme A dehydrogenase deficiency screening test |
|
| 940221000000103 | Maple syrup urine disease screening test |
|
| 940201000000107 | Homocystinuria screening test |
|
| 940151000000102 | Isovaleric acidaemia screening test |
|
| 940131000000109 | Glutaric aciduria type 1 screening test |
|