Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2

MONDO:0018996

A rare autosomal recessive cerebellar ataxia (ARCA), characterized by progressive cerebellar ataxia associated with frequent oculomotor apraxia, severe neuropathy and an elevated serum alpha-fetoprotein (AFP) level.

Also known as: AOA2, SCAN 2, SCAN2, ataxia with oculomotor apraxia type 2, ataxia-ocular apraxia 2, ataxia-oculomotor apraxia 2, ataxia-oculomotor apraxia type 2, spinocerebellar ataxia with axonal neuropathy type 2

29 clinical trials for this condition and its sub-types, 2 tagged with Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 itself.

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↑ Hereditary peripheral neuropathy (479) ↑ Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy (2)

Including sub-types (29) Tagged with Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2 (2)

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Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2

Where it sits in the disease tree

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