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congenital stationary night blindness autosomal dominant 1

http://purl.obolibrary.org/obo/DOID_0110862

A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in mutations in the RHO gene on chromosome 3q22.1. [ http://purl.obolibrary.org/obo/ECO_0007645 ]

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Term info

Label

congenital stationary night blindness autosomal dominant 1

Synonyms

CSNBAD1
rhodopsin-related congenital stationary night blindness

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disease_ontology

DOID:0110862

Term relations

Subclass of:

autosomal dominant disease
congenital stationary night blindness
has material basis in some autosomal dominant inheritance