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| Term | Stevens-Johnson syndrome | ID (Ontology) | DOID:0050426 (Human Disease) |
| 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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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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integumentary system disease |__skin disease |__Stevens-Johnson syndrome |
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| Is a | skin disease | ||
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External Crossreferences & Linkouts
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EFO:0004276 GARD:7700 ICD10CM:L51.1 ICD9CM:695.13 MESH:D013262 NCI:C79484 SNOMEDCT_US_2023_03_01:73442001 UMLS_CUI:C0038325 |
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