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DO Term : congenital nystagmus 1 [DOID:0111790] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene on chromosome Xq26.2.

synonyms:
NYS1,
GARD:2969,
OMIM:310700,
310700,
X-linked infantile nystagmus 1,
congenital motor nystagmus 1

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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