Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2003. Module: SNOMED CT core module
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 1767867012 | Progeroid short stature with pigmented nevi (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
| 1773476012 | Progeroid short stature with pigmented naevi | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 1774762017 | Progeroid short stature with pigmented nevi | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 1787044017 | Baraitser syndrome | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
| 1787045016 | Mulvihill-Smith syndrome | en | Synonym | Active | Only initial character case insensitive | SNOMED CT core module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Progeroid short stature with pigmented nevi | Is a | Premature aging syndrome | true | Inferred relationship | Existential restriction modifier | ||
| Progeroid short stature with pigmented nevi | Occurrence | Congenital | true | Inferred relationship | Existential restriction modifier | 1 | |
| Progeroid short stature with pigmented nevi | Finding site | Skin structure | true | Inferred relationship | Existential restriction modifier | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR