Disease #06962 (RP93 (retinitis pigmentosa, type 93), OMIM:619845)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
Register as submitter | Log in

	Curators: InSiGHT - John-Paul Plazzer, Mev Dominguez Valentin, and Bryony A Thompson

Official abbreviation	RP93
Name	retinitis pigmentosa, type 93
OMIM ID	619845
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CC2D2A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-09-18 13:41:32 +02:00 (CEST)
Date last edited	N/A

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