Disease #05724 (RP79 (retinitis pigmentosa, type 79 (RP79)), OMIM:617460)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Global Variome, with Curator vacancy

Official abbreviation	RP79
Name	retinitis pigmentosa, type 79 (RP79)
OMIM ID	617460
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HK1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-04-10 19:42:29 +02:00 (CEST)
Date last edited	N/A

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