DISEASES

Disease-gene associations mined from literature

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Human genes for basal ganglia disease

Basal ganglia disease [DOID:679]

A brain disease that is characterized by dysfunctional movement, located_in basal ganglia with_material_basis_in diseased components of the basal ganglia and associated neural circuits.

Synonyms:  basal ganglia disease,  basal ganglia disorder,  basal ganglia syndrome,  basal ganglia diseases,  DOID:679

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.