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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 congenital stationary night blindness

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