Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		0.110 GeneticVariation BEFREE Hereditary motor and sensory neuropathy type 2C (HMSN2C, Charcot-Marie-Tooth 2C [CMT2C]) is an autosomal dominant motor and sensory neuropathy involving limb, diaphragm, vocal cord, and intercostal muscles. 12682323

2003
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0151313
Disease: Sensory neuropathy
Sensory neuropathy 		0.110 Biomarker HPO