Disease #05721 (RP76 (retinitis pigmentosa, type 76 (RP76)), OMIM:617123)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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	Curator: Johan den Dunnen

Official abbreviation	RP76
Name	retinitis pigmentosa, type 76 (RP76)
OMIM ID	617123
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	POMGNT1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-04-10 19:39:34 +02:00 (CEST)
Date last edited	N/A

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