Autosomal Recessive Pericentral Pigmentary Retinopathy
Disease ID: disease_node_15825
Connections displayed (default: 10).
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| Dbxref | ICD10CM:H35.5, MIM:268060 |
|---|---|
| Subclassof | DOID_0050737, DOID_10584 |
| Data Source | DOID |
| Doid Label | autosomal recessive pericentral pigmentary retinopathy |
| Doid Description | A retinitis pigmentosa that is characterized autosomal recessive inheritance of pigmentary retinal degeneration with onset in the infancy but slower rates of progression than other forms of retinopathy. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_15825 |
| Doid Id | DOID_0110422 |
| Label | Autosomal Recessive Pericentral Pigmentary Retinopathy |
- 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)