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 |
SNOMEDCT_US_2023_03_01:73442001 UMLS_CUI:C0038325 ICD9CM:695.13 ICD10CM:L51.1 MESH:D013262 EFO:0004276 GARD:7700 NCI:C79484 |
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| 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. |
|
| has close match |
MESH:D013262 |
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| has exact match |
MESH:D013262 |
|
| has_obo_namespace |
disease_ontology |
|
| id |
DOID:0050426 |
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| in_subset | ||
| label |
Stevens-Johnson syndrome |
|
| notation |
DOID:0050426 |
|
| note |
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. |
|
| preferred label |
Stevens-Johnson syndrome |
|
| prefLabel |
Stevens-Johnson syndrome |
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| subClassOf |