Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3433502013 | Congenital ichthyosis with hypotrichosis syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3433503015 | Congenital ichthyosis with hypotrichosis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3433504014 | Ichthyosis, follicular atrophoderma, hypotrichosis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3433505010 | Syndrome with characteristics of congenital ichthyosis and hypotrichosis. It has been described in three members of a consanguineous Arab Israeli family. The syndrome is transmitted as an autosomal recessive trait and is caused by a missense mutation in the ST14 gene, encoding the recently identified protease, matriptase on chromosome 11q24. Analysis of skin samples from the patients suggests that this enzyme plays a role in epidermal desquamation. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3984601000052115 | kongenital iktyos med hypotrikos | sv | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Is a | Congenital hypotrichia | true | Inferred relationship | Some | ||
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Is a | Autosomal recessive ichthyosis (disorder) | true | Inferred relationship | Some | ||
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Associated morphology | kongenital hypoplasi | false | Inferred relationship | Some | 2 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 2 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Finding site | Hair structure (body structure) | false | Inferred relationship | Some | 2 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Associated morphology | utvecklingsabnormitet | false | Inferred relationship | Some | 3 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Occurrence | Congenital | false | Inferred relationship | Some | 3 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 3 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | 2 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 2 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Finding site | Hair structure (body structure) | true | Inferred relationship | Some | 1 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Associated morphology | Hypoplasia | true | Inferred relationship | Some | 1 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Associated morphology | Hyperkeratosis | true | Inferred relationship | Some | 2 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Has interpretation | Abnormal | true | Inferred relationship | Some | 3 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Interprets | Keratinization | true | Inferred relationship | Some | 3 | |
Congenital ichthyosis with hypotrichosis syndrome (disorder) | Finding site | Entire skin | true | Inferred relationship | Some | 2 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets