Disease #03426 (RP45 (retinitis pigmentosa, type 45 (RP45)), OMIM:613767)
Official abbreviation |
RP45 |
Name |
retinitis pigmentosa, type 45 (RP45) |
OMIM ID |
613767 |
Human Phenotype Ontology Project (HPO) |
HPO |
Inheritance |
Autosomal recessive |
Individuals reported having this disease |
- |
Phenotype entries for this disease |
- |
Associated with 1 gene |
CNGB1 |
Associated tissues |
- |
Disease features |
- |
Remarks |
- |
Date created |
2014-09-25 23:29:40 +02:00 (CEST) |
Date last edited |
2021-10-31 14:50:56 +01:00 (CET) |
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|