Retinitis Pigmentosa 88
Disease ID: disease_node_15797
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:618826 |
|---|---|
| Subclassof | DOID_0050737, DOID_10584 |
| Data Source | DOID |
| Synonyms | RP88 |
| Doid Label | retinitis pigmentosa 88 |
| Doid Description | A retinitis pigmentosa characterized by night blindness and constriction of peripheral visual fields, with mildly reduced visual acuity that has_material_basis_in homozygous or compound heterozygous mutation in the RP1L1 gene on chromosome 8p23.1. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15797 |
| Doid Id | DOID_0112145 |
| Label | Retinitis Pigmentosa 88 |
- Outgoing r'ship
SUBCLASS_OFto/from Retinitis Pigmentosa(ID:disease_node_6614) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)