DISEASES

Disease-gene associations mined from literature

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Human genes for autosomal recessive spinocerebellar ataxia 10

Autosomal recessive spinocerebellar ataxia 10 [DOID:0050999]

An autosomal recessive cerebellar ataxia that is characterized by ataxia, dysarthria, nystagmus and marked cerebellar atrophy, has_material_basis_in mutation in the ANO10 gene.

Synonyms:  autosomal recessive spinocerebellar ataxia 10,  DOID:0050999,  SCAR10

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.