| Preferred Name |
遗传性大疱性表皮松解症 / Genetically-determined epidermolysis bullosa |
| Definitions |
Epidermolysis bullosa (EB) is the name given to a heterogeneous group of blistering disorders which in the majority of cases are due to genetically-determined defects in structural proteins of the epidermis and dermo-epidermal junction. The genetic forms are to be distinguished from the immunobullous disorder, epidermolysis bullosa acqiusita (qv). |
| ID |
http://purl.bmicc.cn/ontology/ICD11CN/L2-EC3 |
| definition |
Epidermolysis bullosa (EB) is the name given to a heterogeneous group of blistering disorders which in the majority of cases are due to genetically-determined defects in structural proteins of the epidermis and dermo-epidermal junction. The genetic forms are to be distinguished from the immunobullous disorder, epidermolysis bullosa acqiusita (qv). |
| exclusions |
Epidermolysis bullosa acquisita (EB43) |
| hasDbXref | |
| label |
遗传性大疱性表皮松解症 / Genetically-determined epidermolysis bullosa |
| mappingRelation | |
| notation |
L2-EC3 |
| prefixIRI |
ICD11CN:L2-EC3 |
| prefLabel |
遗传性大疱性表皮松解症 / Genetically-determined epidermolysis bullosa |
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| There are currently no mappings for this class. | |||