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DO Term : congenital stationary night blindness 1A [DOID:0110870] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital stationary night blindness that has_material_basis_in mutation in the NYX gene on chromosome Xp11.4.

synonyms:
complete CSNB X-linked,
310500,
congenital stationary night blindness 1A X-linked,
NBMI,
hemeralopia-myopia,
myopia-night blindness,
congenital stationary night blindness with myopia,
CSNB1A,
OMIM:310500

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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