DISEASES

Disease-gene associations mined from literature

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Human genes for Charcot-Marie-Tooth disease type 1

Charcot-Marie-Tooth disease type 1 [DOID:0050538]

A Charcot-Marie-Tooth disease characterized by demyelination of the peripheral nerve axons.

Synonyms:  Charcot-Marie-Tooth disease type 1,  CharcotMarieTooth disease type 1,  DOID:0050538,  hereditary motor and sensory neuropathy type 1,  familial motor and sensory neuropathy type 1

Linkouts:  OMIM #1 #2 #3 #4 #5 #6

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.