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Metadata
ID	DOID:0110862
Name	congenital stationary night blindness autosomal dominant 1
Definition	A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1. https://www.ncbi.nlm.nih.gov/pubmed/7846071
Xrefs	OMIM:610445
Synonyms	CSNBAD1 [EXACT] rhodopsin-related congenital stationary night blindness [EXACT]
Parent Relationships	is_a autosomal dominant disease is_a congenital stationary night blindness