Disease #04528 (RDGCA (dystrophy, retinal?, with inner retinal dysfunction and ganglion cell abnormalities (RDGCA)), OMIM:616079)

Official abbreviation	RDGCA
Name	dystrophy, retinal?, with inner retinal dysfunction and ganglion cell abnormalities (RDGCA)
OMIM ID	616079
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	ITM2B
Associated tissues	-
Disease features	-
Remarks	-
Date created	2015-09-23 10:25:22 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD