Epidermolysis Bullosa
Disease ID: disease_node_2967
Connections displayed (default: 10).
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| Dbxref | GARD:6359, ICD10CM:Q81, MESH:D004820, NCI:C67383, SNOMEDCT_US_2023_03_01:205580008, UMLS_CUI:C0014527 |
|---|---|
| Subclassof | DOID_2731 |
| Data Source | DOID, MESH |
| Synonyms | acantholysis bullosa |
| Mesh Id | D004820 |
| Mesh Label | Epidermolysis Bullosa |
| Mesh Subclassof | D012872, D012868, D012873 |
| Doid Label | epidermolysis bullosa |
| Doid Description | A vesiculobullous skin disease that is characterized by formation of blisters with only minor skin trauma, which can cause widespread wounds, dehydration, electrolyte abnormalities, and severe infection, frequently develops_from mutations in connective tissue elements, including genes encoding keratin, collagen, and laminin. |
| Disease Node Id | disease_node_2967 |
| Doid Id | DOID_2730 |
| Label | Epidermolysis Bullosa |
- Incoming r'ship
SUBCLASS_OFto/from Epidermolysis Bullosa Simplex(ID:disease_node_8575) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Epidermolysis Bullosa Acquisita(ID:disease_node_8560) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Epidermolysis Bullosa, Junctional(ID:disease_node_8570) (Disease) - Incoming r'ship
SUBCLASS_OFto/from Epidermolysis Bullosa Dystrophica(ID:disease_node_8564) (Disease)