DISEASES

Disease-gene associations mined from literature

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Human genes for Charcot-Marie-Tooth disease type 3

Charcot-Marie-Tooth disease type 3 [DOID:0050540]

A Charcot-Marie-Tooth disease that is characterized by motor and sensory peripheral neuropathies caused by demyelination.

Synonyms:  Charcot-Marie-Tooth disease type 3,  CharcotMarieTooth disease type 3,  DOID:0050540,  DEJERINE-SOTTAS NEUROPATHY,  DEJERINE-SOTTAS SYNDROME ...

Linkouts:  OMIM

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.