limb dysmetria Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of dysmetria involving the limbs. (Human Phenotype Ontology, HP_0002406)
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3 genes associated with the limb dysmetria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GBA2 glucosidase, beta (bile acid) 2
KCNC3 potassium channel, voltage gated Shaw related subfamily C, member 3
SLC20A2 solute carrier family 20 (phosphate transporter), member 2