Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core
Descriptions:
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
An exceedingly rare, autosomal recessive immune disease characterised 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 | Existential restriction modifier (core metadata concept) | |
Aplasia of thumb | Is a | True | Congenital absence of thumb | Inferred relationship | Existential restriction modifier (core metadata concept) |
This concept is not in any reference sets