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 | 
| 378325011 | Hereditary acrosteolysis | en | Synonym | Inactive | Entire term case insensitive | SNOMED CT core module | 
| 644999014 | Hereditary acrosteolysis (disorder) | en | Fully specified name | Inactive | Entire term case insensitive | SNOMED CT core 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