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Vogt-Koyanagi-Harada disease
Summary
- Synonym
-
- Harada's disease
- Vogt-Koyanagi syndrome
- uveomeningoencephalitic syndrome
- Definition
- An autoimmune disease that is caused by T helper cell mediated autoimmune attack of melanocytes resulting in inflammation of the inside of the eye, whitening of hair, skin pigment loss, and meningitis.
- Super Class
- autoimmune disease of skin and connective tissue
External Links
- Disease Ontology
- DOID:12297
- Mondo Disease Ontology
- MeSH
- UMLS
- NCI Thesaurus
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1591 | CYP24A1 | cytochrome P450 family 24 subfamily A member 1 | |
| 6120 | RPE | ribulose-5-phosphate-3-epimerase | |
| 7124 | TNF | tumor necrosis factor | |
| 23274 | CLEC16A | C-type lectin domain containing 16A | |
| 120227 | CYP2R1 | cytochrome P450 family 2 subfamily R member 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q2KHT3 | Protein CLEC16A | |
| Q96AT9 | Ribulose-phosphate 3-epimerase |
