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DO Term : congenital stationary night blindness autosomal dominant 2 [DOID:0110863] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital stationary night blindness characterized by autosomal dominant inheritance that has_material_basis_in heterozygous mutation in the PDE6B gene on chromosome 4p16.

synonyms:
CSNBAD2,
Rambusch type congenital stationary night blindness,
OMIM:163500,
163500

Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents

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