Disease #05722 (RP77 (retinitis pigmentosa, type 77 (RP77)), OMIM:617304)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP77
Name	retinitis pigmentosa, type 77 (RP77)
OMIM ID	617304
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	REEP6
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-04-10 19:40:29 +02:00 (CEST)
Date last edited	N/A

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