Pharc Syndrome
Disease ID: disease_node_20309
Connections displayed (default: 10).
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| Dbxref | MIM:612674, ORDO:171848 |
|---|---|
| Subclassof | DOID_225, DOID_0050737 |
| Data Source | DOID |
| Synonyms | polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract |
| Doid Label | PHARC syndrome |
| Doid Description | A syndrome that is characterized by polyneuropathy, hearing loss, cerebellar ataxia, retinitis pigmentosa and early-onset cataract. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_20309 |
| Doid Id | DOID_0080181 |
| Label | Pharc Syndrome |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Syndrome(ID:disease_node_7213) (Disease)