Retinitis Pigmentosa 86
Disease ID: disease_node_15794
Connections displayed (default: 10).
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| Dbxref | MIM:618613 |
|---|---|
| Subclassof | DOID_10584, DOID_0050739 |
| Data Source | DOID |
| Synonyms | RP86 |
| Doid Label | retinitis pigmentosa 86 |
| Doid Description | A retinitis pigmentosa characterized by night blindness followed by progressive narrowing of visual fields and decline in visual acuity that has_material_basis_in mutation in the KIAA1549 gene on chromosome 7q34. |
| Has Material Basis In | GENO_0000934 |
| Disease Node Id | disease_node_15794 |
| Doid Id | DOID_0112143 |
| Label | Retinitis Pigmentosa 86 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Genetic Disease(ID:disease_node_15586) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Retinitis Pigmentosa(ID:disease_node_6614) (Disease)