Disease #03441 (RP39 (retinitis pigmentosa, type 39 (RP39)), OMIM:613809)
Official abbreviation |
RP39 |
Name |
retinitis pigmentosa, type 39 (RP39) |
OMIM ID |
613809 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
- |
Individuals reported having this disease |
1 |
Phenotype entries for this disease |
1 |
Associated with 1 gene |
USH2A |
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) |
Individuals
|