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 |
3311572010 | Autosomal dominant popliteal pterygium syndrome (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3311573017 | Autosomal dominant popliteal pterygium syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3311574011 | Facio-genito-popliteal syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3311575012 | Popliteal web syndrome | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
3311576013 | A rare genetic malformation disorder with characteristics of cleft lip, with or without cleft palate, contractures of the lower extremities, abnormal external genitalia, syndactyly of fingers and/or toes, and a pyramidal skin fold over the hallux nail. Associated with mutations in the IRF6 gene (1q32.2-q32.3) which is involved in the formation of connective and epithelial tissues. Follows an autosomal dominant pattern of inheritance. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Autosomal dominant popliteal pterygium syndrome (disorder) | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Autosomal dominant popliteal pterygium syndrome (disorder) | Is a | Popliteal pterygium syndrome | true | Inferred relationship | Some | ||
Autosomal dominant popliteal pterygium syndrome (disorder) | Associated morphology | Congenital webbing | true | Inferred relationship | Some | 1 | |
Autosomal dominant popliteal pterygium syndrome (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Autosomal dominant popliteal pterygium syndrome (disorder) | Finding site | Popliteal region structure | true | Inferred relationship | Some | 1 | |
Autosomal dominant popliteal pterygium syndrome (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Autosomal dominant popliteal pterygium syndrome (disorder) | Is a | Developmental hereditary disorder | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets