Disease #00895 (RP61 (retinitis pigmentosa, type 61 (RP61)), OMIM:614180)
| Official abbreviation |
RP61 |
| Name |
retinitis pigmentosa, type 61 (RP61) |
| OMIM ID |
614180 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
CLRN1 |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2020-04-09 15:05:56 +02:00 (CEST) |
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