Disease #05726 (RP81 (retinitis pigmentosa, type 81 (RP81)), OMIM:617871)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP81
Name	retinitis pigmentosa, type 81 (RP81)
OMIM ID	617871
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	IFT43
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-04-10 19:44:30 +02:00 (CEST)
Date last edited	N/A

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