Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
98397018 | Familial porphyria cutanea tarda | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
98398011 | Hereditary porphyria cutanea tarda | en | Synonym (core metadata concept) | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
798048011 | Familial porphyria cutanea tarda (disorder) | en | Fully specified name | Active | Entire term case insensitive (core metadata concept) | SNOMED CT core |
5247305010 | PCT (porphyria cutanea tarda) type II | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Familial porphyria cutanea tarda | Is a | Porphyria cutanea tarda | true | Inferred relationship | Some | ||
Familial porphyria cutanea tarda | Occurrence | Congenital | false | Inferred relationship | Some | ||
Familial porphyria cutanea tarda | Finding site | Skin structure | true | Inferred relationship | Some | 2 | |
Familial porphyria cutanea tarda | Finding site | Liver structure | true | Inferred relationship | Some | 1 | |
Familial porphyria cutanea tarda | Is a | Familial disease | true | Inferred relationship | Some | ||
Familial porphyria cutanea tarda | Is a | Autosomal dominant hereditary disorder | true | Inferred relationship | Some | ||
Familial porphyria cutanea tarda | Is a | Digestive system hereditary disorder (disorder) | true | Inferred relationship | Some | ||
Familial porphyria cutanea tarda | Is a | Hereditary disorder of the integument | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
This concept is not in any reference sets