Retinitis Pigmentosa 87
Disease ID: disease_node_15798
Connections displayed (default: 10).
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| Dbxref | MIM:618697 |
|---|---|
| Subclassof | DOID_0050736, DOID_10584 |
| Data Source | DOID |
| Synonyms | RP87, retinitis pigmentosa 87 with choroidal involvement |
| Doid Label | retinitis pigmentosa 87 |
| Doid Description | A retinitis pigmentosa characterized by slowly progressive visual disturbance and extensive choroid/retinal atrophy that has_material_basis_in heterozygous mutation in the RPE65 gene on chromosome 1p31.3. |
| Has Material Basis In | GENO_0000147 |
| Disease Node Id | disease_node_15798 |
| Doid Id | DOID_0112144 |
| Label | Retinitis Pigmentosa 87 |
- Outgoing r'ship
SUBCLASS_OFto/from Retinitis Pigmentosa(ID:disease_node_6614) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Domit Disease(ID:disease_node_13255) (Disease)