sensorimotor neuropathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007141
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Genes

13 genes associated with the sensorimotor neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABHD12 abhydrolase domain containing 12
AFG3L2 AFG3-like AAA ATPase 2
AMACR alpha-methylacyl-CoA racemase
CLCF1 cardiotrophin-like cytokine factor 1
GALC galactosylceramidase
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
MPV17 MpV17 mitochondrial inner membrane protein
PDYN prodynorphin
PHYH phytanoyl-CoA 2-hydroxylase
PPP2R2B protein phosphatase 2, regulatory subunit B, beta
RPIA ribose 5-phosphate isomerase A
SLC30A10 solute carrier family 30, member 10
SPTLC2 serine palmitoyltransferase, long chain base subunit 2