Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3326199017 | Familial hypertryptophanemia (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 3326200019 | Familial hypertryptophanemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 3326207016 | Familial hypertryptophanaemia | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Familial hypertryptophanemia | Is a | Autosomal recessive hereditary disorder | true | Inferred relationship | Existential restriction modifier | ||
| Familial hypertryptophanemia | Is a | Familial disease | true | Inferred relationship | Existential restriction modifier | ||
| Familial hypertryptophanemia | Is a | Tryptophanemia | true | Inferred relationship | Existential restriction modifier |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR