Disease #06964 (RP92 (retinitis pigmentosa, type 92), OMIM:619614)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP92
Name	retinitis pigmentosa, type 92
OMIM ID	619614
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	HKDC1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-09-18 13:45:44 +02:00 (CEST)
Date last edited	N/A

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