Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3308843016 | Hereditary hypotrichosis simplex of scalp (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3308849017 | Hereditary hypotrichosis simplex of scalp | en | Synonym | Active | Case insensitive | SNOMED CT core |
3308850017 | Hypotrichosis simplex of scalp | en | Synonym | Active | Case insensitive | SNOMED CT core |
3309176013 | Hypotrichosis simplex of the scalp (HSS) has manifestation of diffuse progressive hair loss that is confined to the scalp. Prevalence is unknown but HSS has been described in multiple members (males and females) of several large families. Progressive hair loss generally begins during the first decade of life and most patients are completely bald by the third decade of life. Body, axillary and facial hair, as well as the eyebrows and eyelashes are unaffected. There are no anomalies of the skin, nails and teeth. The causative gene CDSN (encoding the keratinocyte adhesion molecule, corneodesmosin) has been mapped to chromosome 6p21.3. Transmitted in an autosomal dominant manner. | en | Definition | Active | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Hereditary hypotrichosis simplex of scalp | Associated morphology | Growth alteration | true | Inferred relationship | Some | 1 | |
Hereditary hypotrichosis simplex of scalp | Finding site | Hair structure | true | Inferred relationship | Some | 1 | |
Hereditary hypotrichosis simplex of scalp | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Hereditary hypotrichosis simplex of scalp | Is a | Hypotrichosis | false | Inferred relationship | Some | ||
Hereditary hypotrichosis simplex of scalp | Is a | Disorder of scalp | true | Inferred relationship | Some | ||
Hereditary hypotrichosis simplex of scalp | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Hereditary hypotrichosis simplex of scalp | Is a | Disorder of skin of head | true | Inferred relationship | Some | ||
Hereditary hypotrichosis simplex of scalp | Finding site | Skin structure of scalp | true | Inferred relationship | Some | 2 | |
Hereditary hypotrichosis simplex of scalp | Finding site | Hair structure | false | Inferred relationship | Some | ||
Hereditary hypotrichosis simplex of scalp | Is a | Hereditary hypotrichosis simplex | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set