impaired distal vibration sensation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A decrease in the ability to perceive vibration in the distal portions of the limbs. (Human Phenotype Ontology, HP_0006886)
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6 genes associated with the impaired distal vibration sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DCAF8 DDB1 and CUL4 associated factor 8
FMR1 fragile X mental retardation 1
LRSAM1 leucine rich repeat and sterile alpha motif containing 1
POLG polymerase (DNA directed), gamma
PRKCG protein kinase C, gamma
SETX senataxin