Disease #05726 (RP81 (retinitis pigmentosa, type 81 (RP81)), OMIM:617871)

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	RP81
Name	retinitis pigmentosa, type 81 (RP81)
OMIM ID	617871
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	IFT43
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-04-10 19:44:30 +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.