Disease #03159 (RP46 (retinitis pigmentosa, type 46 (RP46)), OMIM:612572)

Official abbreviation RP46
Name retinitis pigmentosa, type 46 (RP46)
OMIM ID 612572
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene IDH3B
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)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.