Nystagmus 4, congenital, autosomal dominant
Other Names for this Disease
- Vestibulocerebellar disorder with predominant ocular signs
On this page
- Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine.
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