Disease #06963 (RP91 (retinitis pigmentosa, type 91), OMIM:153870)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP91
Name	retinitis pigmentosa, type 91
OMIM ID	153870
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	IMPG1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-09-18 13:43:43 +02:00 (CEST)
Date last edited	N/A

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