Disease #00888 (RP55 (retinitis pigmentosa, type 55 (RP55)), OMIM:613575)
| Official abbreviation |
RP55 |
| Name |
retinitis pigmentosa, type 55 (RP55) |
| OMIM ID |
613575 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
- |
| Individuals reported having this disease |
- |
| Phenotype entries for this disease |
- |
| Associated with 1 gene |
ARL6 |
| 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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