Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2021. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 4167012011 | Phenylketonuria due to BH4 deficiency | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| 4167014012 | Phenylketonuria due to tetrahydrobiopterin deficiency | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 4167524012 | Phenylketonuria due to tetrahydrobiopterin deficiency (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Phenylketonuria due to tetrahydrobiopterin deficiency | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Existential restriction modifier | ||
| Phenylketonuria due to tetrahydrobiopterin deficiency | Is a | Hyperphenylalaninemia | false | Inferred relationship | Existential restriction modifier | ||
| Phenylketonuria due to tetrahydrobiopterin deficiency | Due to | Disorder of tetrahydrobiopterin metabolism | true | Inferred relationship | Existential restriction modifier | 1 | |
| Phenylketonuria due to tetrahydrobiopterin deficiency | Is a | Phenylketonuria | true | Inferred relationship | Existential restriction modifier | ||
| Phenylketonuria due to tetrahydrobiopterin deficiency | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR