Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase 890435004
SNOMED CT code
| SNOMED code | 890435004 |
|---|---|
| name | Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase |
| status | active |
| date introduced | 2021-01-31 |
| fully specified name(s) | Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase (disorder) |
| synonyms | Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| parents | Classical phenylketonuria 7573000 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Enzymopathy 78548001 Phenylketonuria 190687004 Classical phenylketonuria 7573000 Classical phenylketonuria with partial deficiency of phenylalanine hydroxylase 890435004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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