DISEASES

Disease-gene associations mined from literature

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Human genes for Charcot-Marie-Tooth disease type 4

Charcot-Marie-Tooth disease type 4 [DOID:0050541]

A Charcot-Marie-Tooth disease characterized by demyelinating or axonal abnormalities that has_material_basis_in autosomal recessive inheritance.

Synonyms:  Charcot-Marie-Tooth disease type 4,  CharcotMarieTooth disease type 4,  DOID:0050541,  hereditary motor and sensory neuropathy,  familial motor and sensory neuropathy ...

Linkouts:  OMIM #1 #2 #3 #4 #5 #6 #7 #8 #9 #10

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.