Disease #05723 (RP78 (retinitis pigmentosa, type 78 (RP78)), OMIM:617433)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP78
Name	retinitis pigmentosa, type 78 (RP78)
OMIM ID	617433
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ARHGEF18
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-04-10 19:41:39 +02:00 (CEST)
Date last edited	N/A

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