impaired distal proprioception Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A loss or impairment of the sensation of the relative position of parts of the body and joint position occuring at distal joints. (Human Phenotype Ontology, HP_0006858)
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2 genes associated with the impaired distal proprioception phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CYP7B1 cytochrome P450, family 7, subfamily B, polypeptide 1
POLG polymerase (DNA directed), gamma