Disease #03946 (RP82 (retinitis pigmentosa, with/without situs inversus (RP82)), OMIM:615434)
| Official abbreviation |
RP82 |
| Name |
retinitis pigmentosa, with/without situs inversus (RP82) |
| OMIM ID |
615434 |
| Human Phenotype Ontology Project (HPO) |
HPO |
| Inheritance |
Autosomal recessive |
| Individuals reported having this disease |
2 |
| Phenotype entries for this disease |
5 |
| Associated with 1 gene |
ARL2BP |
| Associated tissues |
- |
| Disease features |
- |
| Remarks |
- |
| Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
| Date last edited |
2019-12-17 16:21:56 +01:00 (CET) |
Individuals
|