Uveomeningoencephalitic Syndrome
Disease ID: disease_node_7827
Connections displayed (default: 10).
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| Dbxref | GARD:7862, ICD10CM:H20.82, ICD9CM:364.24, MESH:D014607, NCI:C85218, SNOMEDCT_US_2023_03_01:44923005, UMLS_CUI:C0042170 |
|---|---|
| Subclassof | DOID_0060039 |
| Data Source | DOID, MESH |
| Synonyms | Harada's disease, Vogt-Koyanagi syndrome, uveomeningoencephalitic syndrome |
| Disease Has Location | UBERON_0000014, UBERON_0002384 |
| Mesh Id | D014607 |
| Mesh Label | Uveomeningoencephalitic Syndrome |
| Mesh Subclassof | D020274, D014605 |
| Doid Label | Vogt-Koyanagi-Harada disease |
| Doid Description | 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. |
| Has Symptom | SYMP_0019173 |
| Disease Node Id | disease_node_7827 |
| Doid Id | DOID_12297 |
| Label | Uveomeningoencephalitic Syndrome |
- Outgoing r'ship
HAS_SYMPTOMto/from Meningitis(ID:disease_node_5109;disease_node_21406) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autoimmune Disease Of Skin And Connective Tissue(ID:disease_node_14213) (Disease)