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DO Term : congenital nystagmus 2 [DOID:0111792] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A congenital nystagmus that has_material_basis_in heterozygous mutation in a region of chromosome 6p12.

synonyms:
congenital motor nystagmus 2,
autosomal dominant congenital nystagmus 2,
NYS2,
OMIM:164100,
GARD:9599,
164100

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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