Disease #03366 (RP57 (retinitis pigmentosa, type 57 (RP57)), OMIM:613582)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP57
Name	retinitis pigmentosa, type 57 (RP57)
OMIM ID	613582
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PDE6G
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2020-08-30 09:26:24 +02:00 (CEST)

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