Retinitis Pigmentosa 56
Disease ID: disease_node_15811
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:H35.5, MIM:613581 |
|---|---|
| Subclassof | DOID_10584, DOID_0050737 |
| Data Source | DOID |
| Synonyms | RP56 |
| Doid Label | retinitis pigmentosa 56 |
| Doid Description | A retinitis pigmentosa that has_material_basis_in mutation in the IMPG2 gene on chromosome 3q12.3. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15811 |
| Doid Id | DOID_0110371 |
| Label | Retinitis Pigmentosa 56 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Retinitis Pigmentosa(ID:disease_node_6614) (Disease)