Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
357808018 | Loose anagen hair syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
627655018 | Loose anagen hair syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
998571000172119 | maladie des cheveux anagènes caducs | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
3387771001000112 | Lose Anagenhaar-Syndrom | de | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Loose anagen hair syndrome | Is a | Disturbance of hair cycle | true | Inferred relationship | Some | ||
Loose anagen hair syndrome | Finding site | Skin structure | false | Inferred relationship | Some | ||
Loose anagen hair syndrome | Finding site | Skin appendage structure (body structure) | false | Inferred relationship | Some | ||
Loose anagen hair syndrome | Finding site | Skin structure | false | Inferred relationship | Some | ||
Loose anagen hair syndrome | Finding site | Hair structure (body structure) | false | Inferred relationship | Some | ||
Loose anagen hair syndrome | Finding site | Skin appendage structure (body structure) | false | Inferred relationship | Some | ||
Loose anagen hair syndrome | Associated morphology | Growth alteration | true | Inferred relationship | Some | 1 | |
Loose anagen hair syndrome | Finding site | Hair structure (body structure) | true | Inferred relationship | Some | 1 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
A Noonan-related syndrome, characterized by facial anomalies suggestive of Noonan syndrome, loose anagen hair, frequent congenital heart defects, distinctive skin features (darkly pigmented skin, keratosis pilaris, eczema or icthyosis), and short stature that is often associated with a growth hormone deficiency. Psychomotor delay with attention deficit/hyperactivity disorder (ADHD) is frequently observed. | Is a | True | Loose anagen hair syndrome | Inferred relationship | Some |
This concept is not in any reference sets