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Metadata
ID	DOID:0110715
Name	congenital stationary night blindness autosomal dominant 3
Definition	A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the GNAT1 gene on chromosome 3p21. https://www.ncbi.nlm.nih.gov/pubmed/8673138
Xrefs	OMIM:610444
Synonyms	CSNBAD3 [EXACT] Nougaret type congenital stationary night blindness [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a congenital stationary night blindness