Disease #05687 (RP75 (retinitis pigmentosa, type 75 (RP75)), OMIM:617023)

Global Variome shared LOVD

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

	Curator: Global Variome, with Curator vacancy

Official abbreviation	RP75
Name	retinitis pigmentosa, type 75 (RP75)
OMIM ID	617023
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	AGBL5
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-01-26 21:19:51 +01:00 (CET)
Date last edited	N/A

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