Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
| Id | Description | Lang | Type | Status | Case? | Module |
| 3008946013 | Legius syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3009354011 | Neurofibromatosis type 1-like syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 3009678012 | NFLS - neurofibromatosis type 1-like syndrome | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
| 3009772019 | Neurofibromatosis type 1-like syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
| 5452221000241117 | syndrome de pseudoneurofibromatose de type 1 | fr | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT Switzerland NRC maintained Module |
| Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
| Legius syndrome | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
| Legius syndrome | Is a | Café au lait spots | true | Inferred relationship | Some | ||
| Legius syndrome | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some | ||
| Legius syndrome | Associated morphology | Pigment alteration | false | Inferred relationship | Some | 1 | |
| Legius syndrome | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
| Legius syndrome | Is a | Genetic disorder of skin pigmentation (disorder) | true | Inferred relationship | Some | ||
| Legius syndrome | Is a | Hyperpigmentation of skin | true | Inferred relationship | Some | ||
| Legius syndrome | Is a | Congenital disease (disorder) | true | Inferred relationship | Some | ||
| Legius syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
| Legius syndrome | Associated morphology | Hyperpigmentation | true | Inferred relationship | Some | 1 |
| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets
FHIR