motor polyneuropathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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5 genes associated with the motor polyneuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CTDP1 CTD (carboxy-terminal domain, RNA polymerase II, polypeptide A) phosphatase, subunit 1
GJC2 gap junction protein, gamma 2, 47kDa
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
SPG11 spastic paraplegia 11 (autosomal recessive)
TRPV4 transient receptor potential cation channel, subfamily V, member 4