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Disease Ontology Browser
autosomal recessive congenital nystagmus (DOID:0111797)
Alliance: disease page
Synonyms: autosomal recessive congenital motor nystagmus
Alt IDs: OMIM:257400
Definition: A congenital nystagmus characterized by autosomal recessive inheritance.

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 6.20
The Jackson Laboratory