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Summary Literature (0)
MIM:606002 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY 2; SCAN2

Xenbase Genes: setx

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011623 - obsolete spinocerebellar ataxia, autosomal recessive 1
MONDO:0018996 - spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2

Disease Ontology (DO):
DOID:0050755 - spinocerebellar ataxia with axonal neuropathy 2