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vitiligo
Summary
- Definition
- An autoimmune disease that causes depigmentation of patches of skin resulting from loss of function or death of melanoctyes.
- Super Class
- autoimmune disease of skin and connective tissue
External Links
- Disease Ontology
- DOID:12306
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- OMIM
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1589 | CYP21A2 | cytochrome P450 family 21 subfamily A member 2 | |
| 1636 | ACE | angiotensin I converting enzyme | |
| 2539 | G6PD | glucose-6-phosphate dehydrogenase | |
| 2876 | GPX1 | glutathione peroxidase 1 | |
| 3383 | ICAM1 | intercellular adhesion molecule 1 | |
| 3821 | KLRC1 | killer cell lectin like receptor C1 | |
| 3992 | FADS1 | fatty acid desaturase 1 | |
| 4153 | MBL2 | mannose binding lectin 2 | |
| 4758 | NEU1 | neuraminidase 1 | |
| 5226 | PGD | phosphogluconate dehydrogenase |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9NPH2 | Inositol-3-phosphate synthase 1 | |
| Q9NZN1 | Interleukin-1 receptor accessory protein-like 1 |
