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Stevens-Johnson syndrome
Summary
- 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.
- Super Class
- skin disease
External Links
- Disease Ontology
- DOID:0050426
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 35 | ACADS | acyl-CoA dehydrogenase short chain | |
| 142 | PARP1 | poly(ADP-ribose) polymerase 1 | |
| 231 | AKR1B1 | aldo-keto reductase family 1 member B | |
| 240 | ALOX5 | arachidonate 5-lipoxygenase | |
| 945 | CD33 | CD33 molecule | |
| 1555 | CYP2B6 | cytochrome P450 family 2 subfamily B member 6 | |
| 1557 | CYP2C19 | cytochrome P450 family 2 subfamily C member 19 | |
| 1559 | CYP2C9 | cytochrome P450 family 2 subfamily C member 9 | |
| 1576 | CYP3A4 | cytochrome P450 family 3 subfamily A member 4 | |
| 2348 | FOLR1 | folate receptor alpha |
Related Glycoprotein
