Retinitis Pigmentosa 49
Disease ID: disease_node_15807
Connections displayed (default: 10).
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| Dbxref | ICD10CM:H35.5, MIM:613756 |
|---|---|
| Subclassof | DOID_10584 |
| Data Source | DOID |
| Synonyms | RP49 |
| Doid Label | retinitis pigmentosa 49 |
| Doid Description | A retinitis pigmentosa that has_material_basis_in mutation in the CNGA1 gene on chromosome 4p12. |
| Disease Node Id | disease_node_15807 |
| Doid Id | DOID_0110377 |
| Label | Retinitis Pigmentosa 49 |
- Outgoing r'ship
SUBCLASS_OFto/from Retinitis Pigmentosa(ID:disease_node_6614) (Disease)