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DO Term : congenital stationary night blindness 2A [DOID:0110871] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital stationary night blindness that has_material_basis_in mutation in the CACNA1F gene on chromosome Xp11.23.

synonyms:
OMIM:300071,
300071,
congenital stationary night blindness 2A X-linked

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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