congenital nystagmus 1

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Summary

Literature (0)

DOID:0111790 - congenital nystagmus 1

Disease Ontology Definition:A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene on chromosome Xq26.2.

Synonyms: congenital motor nystagmus 1, NYS1, X-linked infantile nystagmus 1

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: frmd7

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal genetic disease (is_a), congenital nystagmus (is_a)