Disease #05703 (RP86 (retinitis pigmentosa, type 86 (RP86)), OMIM:618613)

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	RP86
Name	retinitis pigmentosa, type 86 (RP86)
OMIM ID	618613
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	KIAA1549
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-02-26 09:54:29 +01:00 (CET)
Date last edited	N/A

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