Disease #06962 (RP93 (retinitis pigmentosa, type 93), OMIM:619845)

Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ]
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Official abbreviation	RP93
Name	retinitis pigmentosa, type 93
OMIM ID	619845
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal recessive
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	CC2D2A
Associated tissues	-
Disease features	-
Remarks	-
Date created	2022-09-18 13:41:32 +02:00 (CEST)
Date last edited	N/A

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