Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3779271013 | Congenital wooly hair (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3779272018 | Congenital wooly hair | en | Synonym | Active | Case insensitive | SNOMED CT core |
378460016 | Congenital woolly hair | en | Synonym | Active | Case insensitive | SNOMED CT core |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Skin fragillity, woolly hair, palmoplantar keratoderma syndrome | Is a | True | Congenital woolly hair | Inferred relationship | Some | |
Autosomal dominant familial woolly hair | Is a | True | Congenital woolly hair | Inferred relationship | Some | |
Autosomal recessive familial woolly hair | Is a | True | Congenital woolly hair | Inferred relationship | Some | |
Naxos disease | Is a | False | Congenital woolly hair | Inferred relationship | Some | |
Woolly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome | Is a | False | Congenital woolly hair | Inferred relationship | Some | |
Woolly hair with palmoplantar keratoderma syndrome | Is a | False | Congenital woolly hair | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set