DISEASES

Disease-gene associations mined from literature

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Human genes for hereditary sensory neuropathy type 4

Hereditary sensory neuropathy type 4 [DOID:0070146]

A hereditary sensory neuropathy characterized by insensitivity to pain and anhidrosis that has_material_basis_in homozygous or compound heterozygous mutation in the NTRK1 gene on chromosome 1q23.

Synonyms:  hereditary sensory neuropathy type 4,  DOID:0070146,  familial sensory neuropathy type 4,  hereditary sensory neuropathy type IV,  insensitivity to pain, congenital, with anhidrosis ...

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.