DISEASES

Disease-gene associations mined from literature

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Human genes for amyotrophic lateral sclerosis type 15

Amyotrophic lateral sclerosis type 15 [DOID:0060206]

An amyotrophic lateral sclerosis that has_material_basis_in mutation in the UBQLN2 gene on chromosome X.

Synonyms:  amyotrophic lateral sclerosis type 15,  DOID:0060206,  ALS15,  amyotrophic lateral sclerosis 15,  amyotrophic lateral sclerosis 15, 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.