DISEASES

Disease-gene associations mined from literature

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Human genes for amyotrophic lateral sclerosis type 10

Amyotrophic lateral sclerosis type 10 [DOID:0060201]

An amyotrophic lateral sclerosis that has_material_basis_in mutation in the TARDBP gene on chromosome 1.

Synonyms:  amyotrophic lateral sclerosis type 10,  DOID:0060201,  ALS10,  amyotrophic lateral sclerosis 10,  amyotrophic lateral sclerosis 10, with or without frontotemporal dementia ...

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.