loading...| Preferred Name |
Stevens-Johnson syndrome |
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| Synonyms |
|
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| Definitions |
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. |
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| ID |
http://purl.obolibrary.org/obo/DOID_0050426 |
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| database_cross_reference |
UMLS_CUI:C0038325 SNOMEDCT_US_2020_03_01:73442001 ICD9CM:695.13 ICD10CM:L51.1 EFO:0004276 GARD:7700 NCI:C79484 NCI:C79777 |
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| has exact match |
MESH:D013262 |
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| has_obo_namespace |
disease_ontology |
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| id |
DOID:0050426 |
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| imported from | ||
| in_subset | ||
| label |
Stevens-Johnson syndrome |
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| notation |
DOID:0050426 |
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| prefLabel |
Stevens-Johnson syndrome |
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| textual definition |
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. |
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| subClassOf |
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