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DO Term : congenital nystagmus 6 [DOID:0111795] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital nystagmus that has_material_basis_in hemizygous of homoxygous mutation in the GPR143 gene on chromosome Xp22.2.

synonyms:
NYS6,
OMIM:300814,
X-linked congenital nystagmus 6,
300814

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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