DISEASES

Disease-gene associations mined from literature

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Human genes for amyotrophic lateral sclerosis type 13

Amyotrophic lateral sclerosis type 13 [DOID:0060204]

An amyotrophic lateral sclerosis where a mutation that has_material_basis_in the ATXN2 gene on chromosome 12 contributes to suscepitbility.

Synonyms:  amyotrophic lateral sclerosis type 13,  DOID:0060204,  ALS13,  amyotrophic lateral sclerosis 13

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.