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DO Term : congenital nystagmus 5 [DOID:0111796] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital nystagmus that has_material_basis_in hemizygous or heterozygous mutation in a region of chromosome Xp11.4.

synonyms:
OMIM:300589,
NYS5,
300589,
X-linked congenital nystagmus 5

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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