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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
02/13/2024
MGI 6.23
The Jackson Laboratory