Disease #00386 (RP37 (retinitis pigmentosa, type 37 (RP37)), OMIM:611131)

Global Variome shared LOVD

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

Official abbreviation	RP37
Name	retinitis pigmentosa, type 37 (RP37)
OMIM ID	611131
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant, Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	NR2E3
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-05-28 08:39:26 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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