Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3776724019 | Hereditary acroosteolysis (disorder) | en | Fully specified name | Active | Entire term case insensitive | SNOMED CT core module |
3776725018 | Hereditary acroosteolysis | en | Synonym | Active | Entire term case insensitive | SNOMED CT core module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Acroosteolysis, keloid-like lesions, premature aging syndrome | Is a | True | Hereditary acroosteolysis | Inferred relationship | Existential restriction modifier | |
Hypotrichosis, osteolysis, periodontitis, palmoplantar keratoderma syndrome | Is a | True | Hereditary acroosteolysis | Inferred relationship | Existential restriction modifier | |
Giacci familial neurogenic acroosteolysis | Is a | True | Hereditary acroosteolysis | Inferred relationship | Existential restriction modifier |
This concept is not in any reference sets