Status: current, Primitive. Date: 31-Jul 2017. Module: SNOMED CT core
Descriptions:
Id | Description | Lang | Type | Status | Case? | Module |
3432831012 | Junctional epidermolysis bullosa non-Herlitz type (disorder) | en | Fully specified name | Active | Initial character case insensitive | SNOMED CT core |
3432832017 | Junctional epidermolysis bullosa non-Herlitz type | en | Synonym | Active | Initial character case insensitive | SNOMED CT core |
3432833010 | A subtype of junctional epidermolysis bullosa (JEB) with characteristics of skin and mucosal blistering, nail dystrophy or nail absence and enamel hypoplasia. Postinflammatory hypopigmentation or dyspigmentation may be striking in some patients. A generalized subtype with atrophic scarring and more extensive extracutaneous involvement has been described as well as a milder localized subtype. Caused by mutations in the COL17A1 (10q24.3) and LAMA3 (18q11.2), LAMB3 (1q32) and LAMC2 (1q25-q31) genes. The condition follows an autosomal recessive pattern of inheritance. | en | Definition | Inactive | Case sensitive | SNOMED CT core |
3432834016 | A subtype of junctional epidermolysis bullosa (JEB) with characteristics of skin and mucosal blistering, nail dystrophy or nail absence and enamel hypoplasia. Postinflammatory hypopigmentation or dyspigmentation may be striking in some patients. A generalised subtype with atrophic scarring and more extensive extracutaneous involvement has been described as well as a milder localised subtype. Caused by mutations in the COL17A1 (10q24.3) and LAMA3 (18q11.2), LAMB3 (1q32) and LAMC2 (1q25-q31) genes. The condition follows an autosomal recessive pattern of inheritance. | en | Definition | Inactive | Case sensitive | SNOMED CT core |
Outbound Relationships | Type | Target | Active | Characteristic | Refinability | Group | Values |
Junctional epidermolysis bullosa non-Herlitz type | Finding site | Skin structure | true | Inferred relationship | Some | 1 | |
Junctional epidermolysis bullosa non-Herlitz type | Associated morphology | Epidermolysis | true | Inferred relationship | Some | 1 | |
Junctional epidermolysis bullosa non-Herlitz type | Occurrence | Congenital | true | Inferred relationship | Some | 1 | |
Junctional epidermolysis bullosa non-Herlitz type | Pathological process | Pathological developmental process | true | Inferred relationship | Some | 1 | |
Junctional epidermolysis bullosa non-Herlitz type | Is a | Autosomal recessive hereditary disorder | false | Inferred relationship | Some | ||
Junctional epidermolysis bullosa non-Herlitz type | Is a | Inherited disorder of connective tissue | false | Inferred relationship | Some | ||
Junctional epidermolysis bullosa non-Herlitz type | Is a | Hereditary disorder of the integument | false | Inferred relationship | Some | ||
Junctional epidermolysis bullosa non-Herlitz type | Is a | Junctional epidermolysis bullosa | true | Inferred relationship | Some | ||
Junctional epidermolysis bullosa non-Herlitz type | Finding site | Connective tissue structure | false | Inferred relationship | Some | ||
Junctional epidermolysis bullosa non-Herlitz type | Finding site | Skin structure | false | Inferred relationship | Some | 3 | |
Junctional epidermolysis bullosa non-Herlitz type | Finding site | Skin structure | false | Inferred relationship | Some | 4 | |
Junctional epidermolysis bullosa non-Herlitz type | Associated morphology | Epidermolysis | false | Inferred relationship | Some | 3 | |
Junctional epidermolysis bullosa non-Herlitz type | Associated morphology | Developmental abnormality | false | Inferred relationship | Some | 4 | |
Junctional epidermolysis bullosa non-Herlitz type | Occurrence | Congenital | false | Inferred relationship | Some | 4 |
Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group |
Junctional epidermolysis bullosa mitis | Is a | True | Junctional epidermolysis bullosa non-Herlitz type | Inferred relationship | Some | |
Localised non-Herlitz junctional epidermolysis bullosa | Is a | True | Junctional epidermolysis bullosa non-Herlitz type | Inferred relationship | Some |
Reference Sets
Australian emergency department reference set
Clinical finding foundation reference set
Problem/Diagnosis reference set