Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
405470013 | Congenital absence of thumb | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
663349017 | Congenital absence of thumb (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5111001000241115 | absence congénitale du pouce | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
An exceedingly rare, autosomal recessive immune disease characterized by thumb aplasia, short stature with skeletal abnormalities, and combined immunodeficiency described in three sibships from two possibly related families. The skeletal abnormalities included unfused olecranon and the immunodeficiency manifested with severe chickenpox and chronic candidiasis. No new cases have been reported since 1978. | Is a | False | Congenital absence of thumb | Inferred relationship | Some | |
Aplasia of thumb | Is a | True | Congenital absence of thumb | Inferred relationship | Some | |
Congenital absence of nail unit of thumb (disorder) | Is a | True | Congenital absence of thumb | Inferred relationship | Some |
Reference Sets
Description inactivation indicator reference set