Disease #02942 (CSNBAD3 (blindness, night, stationary, congenital, autosomal dominant, type 3 (CSNBAD-3)), OMIM:610444)

Official abbreviation	CSNBAD3
Name	blindness, night, stationary, congenital, autosomal dominant, type 3 (CSNBAD-3)
OMIM ID	610444
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	GNAT1
Associated tissues	-
Disease features	-
Remarks	-
Date created	2014-09-25 23:29:40 +02:00 (CEST)
Date last edited	2021-12-10 21:51:32 +01:00 (CET)

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Global Variome shared LOVD