autosomal recessive congenital nystagmus 8 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive congenital nystagmus 8 (DOID:0061178)
Alliance: disease page
Alt IDs: OMIM:257400
Definition: A congenital nystagmus that has_material_basis_in mutation in the FRMD7 gene on chromosome Xq26.2.

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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