DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for Charcot-Marie-Tooth disease type 4G

Charcot-Marie-Tooth disease type 4G [DOID:0110196]

A Charcot-Marie-Tooth disease type 4 that has_material_basis_in homozygous mutation in the HK1 gene on chromosome 10q22.

Synonyms:  Charcot-Marie-Tooth disease type 4G,  CharcotMarieTooth disease type 4G,  DOID:0110196,  autosomal recessive Charcot-Marie-Tooth disease type 4G,  Charcot-Marie-Tooth neuropathy type 4G ...

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.