Status: current, Primitive. Date: 31-Jul 2014. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3008946013 | Legius syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3009354011 | Neurofibromatosis type 1-like syndrome (disorder) | en | Fully specified name | Active | Case insensitive | SNOMED CT core |
3009678012 | NFLS - neurofibromatosis type 1-like syndrome | en | Synonym | Active | Case sensitive | SNOMED CT core |
3009772019 | Neurofibromatosis type 1-like syndrome | en | Synonym | Active | Case insensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Legius syndrome | Is a | Hyperpigmentation of skin | true | Inferred relationship | Some | ||
Legius syndrome | Is a | Congenital disease | true | Inferred relationship | Some | ||
Legius syndrome | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Legius syndrome | Associated morphology | Hyperpigmentation | true | Inferred relationship | Some | 1 | |
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 | 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