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 |
5401734010 | A rare genetic, multiple congenital anomalies syndrome characterized by cleft lip, with or without cleft palate, pits in the lower lip, contractures of the lower extremities, abnormal external genitalia, syndactyly of fingers and/or toes, and a pyramidal skin fold over the hallux nail. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
5401735011 | A rare genetic, multiple congenital anomalies syndrome characterised by cleft lip, with or without cleft palate, pits in the lower lip, contractures of the lower extremities, abnormal external genitalia, syndactyly of fingers and/or toes, and a pyramidal skin fold over the hallux nail. | 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 |
Reference Sets
Component annotation with string value reference set (foundation metadata concept)