DISEASES

Disease-gene associations mined from literature

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Human genes for Charcot-Marie-Tooth disease axonal type 2U

Charcot-Marie-Tooth disease axonal type 2U [DOID:0110173]

A Charcot-Marie-Tooth disease type 2 that has_material_basis_in heterozygous mutation in the MARS gene on chromosome 12q13.

Synonyms:  Charcot-Marie-Tooth disease axonal type 2U,  CharcotMarieTooth disease axonal type 2U,  DOID:0110173,  autosomal dominant axonal Charcot-Marie-Tooth disease type 2U,  autosomal dominant Charcot-Marie-Tooth disease type 2U ...

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.