Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2016. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3304397019 | Gingival fibromatosis and hypertrichosis syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3304398012 | Gingival fibromatosis and hypertrichosis syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3304404019 | Hirsutism congenital gingival hyperplasia syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 6359291000146116 | CGHT | nl | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6943821000146110 | syndroom van gingivale fibromatose en hypertrichose | nl | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 6943831000146112 | syndroom van gingivale fibromatose en hypertrichose (aandoening) | nl | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Netherlands NRC maintained module (core metadata concept) |
| 3304405018 | A rare autosomal dominant disorder characterized by a generalized enlargement of the gingiva occurring at birth or during childhood that is associated with generalized hypertrichosis developing at birth, during the first years of life, or at puberty and predominantly affecting the face, upper limbs, and midback. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3304406017 | A rare autosomal dominant disorder characterised by a generalised enlargement of the gingiva occurring at birth or during childhood that is associated with generalised hypertrichosis developing at birth, during the first years of life, or at puberty and predominantly affecting the face, upper limbs, and midback. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Gingival fibromatosis and hypertrichosis syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Gingival fibromatosis and hypertrichosis syndrome (disorder) | Is a | Hypertrichosis | true | Inferred relationship | Some | ||
| Gingival fibromatosis and hypertrichosis syndrome (disorder) | Is a | Hereditary gingival fibromatosis | true | Inferred relationship | Some | ||
| Gingival fibromatosis and hypertrichosis syndrome (disorder) | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| Gingival fibromatosis and hypertrichosis syndrome (disorder) | Finding site | Skin structure | false | Inferred relationship | Some | ||
| Gingival fibromatosis and hypertrichosis syndrome (disorder) | Finding site | Hair structure (body structure) | false | Inferred relationship | Some | ||
| Gingival fibromatosis and hypertrichosis syndrome (disorder) | Associated morphology | Fibromatosis | true | Inferred relationship | Some | 3 | |
| Gingival fibromatosis and hypertrichosis syndrome (disorder) | Finding site | Gingival structure | true | Inferred relationship | Some | 3 | |
| Gingival fibromatosis and hypertrichosis syndrome (disorder) | Associated morphology | Growth alteration | true | Inferred relationship | Some | 2 | |
| Gingival fibromatosis and hypertrichosis syndrome (disorder) | Finding site | Hair structure (body structure) | true | Inferred relationship | Some | 2 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets
Description inactivation indicator reference set
FHIR