DISEASES

Disease-gene associations mined from literature

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Human genes for frontotemporal dementia and/or amyotrophic lateral sclerosis-1

Frontotemporal dementia and/or amyotrophic lateral sclerosis-1 [DOID:0060213]

An amyotrophic lateral sclerosis that has_material_basis_in mutation in the C9ORF72 gene on chromosome 9. It is characterized by adult onset of either frontotemporal dementia and/or amyotrophic lateral sclerosis.

Synonyms:  frontotemporal dementia and/or amyotrophic lateral sclerosis-1,  DOID:0060213,  frontotemporal dementia and/or amyotrophic lateral sclerosis1,  ALSFTD,  amyotrophic lateral sclerosis and/or 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.