Status: current, Primitive. Date: 31-Jan 2021. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
4012570010 | Brachydactyly type A3 (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
4012571014 | Brachydactyly type A3 | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
4016120019 | A congenital malformation characterised by shortening of the middle phalanx of the fifth finger. Inherited as an autosomal dominant trait. | en | Definition | Active | Case sensitive | SNOMED CT core |
4016123017 | A congenital malformation characterized by shortening of the middle phalanx of the fifth finger. Inherited as an autosomal dominant trait. | en | Definition | Active | Case sensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Clinical finding foundation reference set
Musculoskeletal finding reference set
Problem/Diagnosis reference set