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Disease Ontology Browser
congenital nystagmus 1 (DOID:0111790)
Alliance: disease page
Synonyms: congenital motor nystagmus 1; NYS1; X-linked infantile nystagmus 1
Alt IDs: OMIM:310700
Definition: A congenital nystagmus that has_material_basis_in mutation in FRMD7 on chromosome Xq26.2.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
MGI 6.21
The Jackson Laboratory