Stevens-Johnson Syndrome
Disease ID: disease_node_7097
Connections displayed (default: 10).
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| Dbxref | EFO:0004276, GARD:7700, ICD10CM:L51.1, ICD9CM:695.13, MESH:D013262, NCI:C79484, SNOMEDCT_US_2023_03_01:73442001, UMLS_CUI:C0038325 |
|---|---|
| Subclassof | DOID_37 |
| Data Source | DOID, MESH |
| Mesh Id | D013262 |
| Mesh Label | Stevens-Johnson Syndrome |
| Mesh Subclassof | D006968, D013280, D004892, D003875 |
| Doid Label | Stevens-Johnson syndrome |
| Doid Description | A skin disease that is characterized by ulceration of less than 10 percent of the surface area of the body. The disease is often precipitated by the use of medications, such as antibiotics or antiepileptics, or onset of infection. |
| Disease Node Id | disease_node_7097 |
| Doid Id | DOID_0050426 |
| Label | Stevens-Johnson Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Skin Diseases(ID:disease_node_6968) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Skin Diseases, Genetic(ID:disease_node_6970) (Disease)