Disease #01471 (CSNBAD2 (blindness, night, stationary, congenital, autosomal dominant, type 2 (CSNBAD-2)), OMIM:163500)

Official abbreviation	CSNBAD2
Name	blindness, night, stationary, congenital, autosomal dominant, type 2 (CSNBAD-2)
OMIM ID	163500
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	PDE6B
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