Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3723743011 | Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | en | Fully specified name | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3723744017 | Epidermolysis bullosa simplex due to BP230 deficiency | en | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT core |
3723747012 | DST (dystonin) related epidermolysis bullosa simplex | en | Synonym (core metadata concept) | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3723742018 | A rare hereditary basal epidermolysis bullosa simplex characterized by mild, predominantly acral, trauma-induced skin fragility, resulting in blisters. Blisters mostly affect the feet, including the dorsal side, and are often several centimeters big. There is evidence the disease is caused by homozygous mutation in the DST (BPAG1) gene on chromosome 6p12. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
3723745016 | A rare hereditary basal epidermolysis bullosa simplex characterised by mild, predominantly acral, trauma-induced skin fragility, resulting in blisters. Blisters mostly affect the feet, including the dorsal side, and are often several centimetres big. There is evidence the disease is caused by homozygous mutation in the DST (BPAG1) gene on chromosome 6p12. | en | Definition | Active | Entire term case sensitive (core metadata concept) | SNOMED CT core |
4208751000052115 | epidermolysis bullosa simplex orsakad av BP230-brist | sv | Synonym (core metadata concept) | Active | Only initial character case insensitive (core metadata concept) | SNOMED CT Sweden NRC maintained module (core metadata concept) |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | Is a | Connective tissue hereditary disorder (disorder) | false | Inferred relationship | Some | ||
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | Finding site | Connective tissue structure | false | Inferred relationship | Some | ||
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | Is a | Epidermolysis bullosa simplex | false | Inferred relationship | Some | ||
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | Associated morphology | Epidermolysis | true | Inferred relationship | Some | 1 | |
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | Pathological process (attribute) | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Epidermolysis bullosa simplex due to BP230 deficiency (disorder) | Is a | Autosomal recessive epidermolysis bullosa simplex | true | Inferred relationship | Some |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Reference Sets