DISEASES

Disease-gene associations mined from literature

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Human genes for Parkinson's disease 22

Parkinson's disease 22 [DOID:0080504]

A late onset Parkinson's disease that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the coiled-coil-helix-coiled-coil-helix domain containing 2 gene on chromosome 7p11.2.

Synonyms:  Parkinson's disease 22,  DOID:0080504,  Parkinsons disease 22,  autosomal dominant Parkinson's disease 22,  autosomal dominant Parkinsons disease 22

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.