DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for Charcot-Marie-Tooth disease type 2A2A

Charcot-Marie-Tooth disease type 2A2A [DOID:0110155]

A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the MFN2 gene on chromosome 1p36.22.

Synonyms:  Charcot-Marie-Tooth disease type 2A2A,  CharcotMarieTooth disease type 2A2A,  DOID:0110155,  autosomal dominant axonal Charcot-Marie-Tooth disease type 2A2,  Charcot-Marie-Tooth neuronal type 2A2 ...

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.