/spinocerebellar ataxia 27A

spinocerebellar ataxia 27A

Rare Disease

MONDO:0008654

Also Known As

NYS4NYSTAGMUS 4, congenital, autosomal dominantnystagmus 4, congenital, autosomal dominantvestibulocerebellar disorder with predominant ocular signs

Comprehensive, easy-to-understand information about this condition

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Gene data from MyGene.info • Click to view on NCBI Gene

GRID2-related autosomal dominant spinocerebellar ataxia

MONDO:0000563

nystagmus 2, congenital, autosomal dominant

MONDO:0008106

nystagmus, hereditary vertical

MONDO:0008107

nystagmus, congenital, autosomal recessive

MONDO:0009762

nystagmus 5, congenital, X-linked

MONDO:0010369

nystagmus 6, congenital, X-linked

MONDO:0010435