Disease #00168 (polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract (PHARC), OMIM:612674)
| Official abbreviation |
- |
| Name |
polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract (PHARC) |
| OMIM ID |
612674 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ABHD12 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2013-07-29 22:25:56 +02:00 (CEST) |
| Date last edited |
N/A |
|
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