Constrictive Median Neuropathy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Injury to the median nerve caused by its entrapment at the wrist as it traverses through the carpal tunnel. Clinically, constrictive median neuropathy is characterized by pain, paresthesia, and weakness in the median nerve distribution of the hand. (Human Phenotype Ontology, HP_0012185)
External Link https://www.disgenet.org/browser/0/1/0/C4023009
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Genes

8 genes associated with the disease Constrictive Median Neuropathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ARSB arylsulfatase B
COL5A1 collagen, type V, alpha 1
GNAS GNAS complex locus
GNPTAB N-acetylglucosamine-1-phosphate transferase, alpha and beta subunits
GSN gelsolin
IDUA iduronidase, alpha-L-
SH3TC2 SH3 domain and tetratricopeptide repeats 2
TTR transthyretin