Disease #05725 (RP80 (retinitis pigmentosa, type 80 (RP80)), OMIM:617781)

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	RP80
Name	retinitis pigmentosa, type 80 (RP80)
OMIM ID	617781
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	IFT140
Associated tissues	-
Disease features	-
Remarks	-
Date created	2020-04-10 19:43:17 +02:00 (CEST)
Date last edited	N/A

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