hypokinesia Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Abnormally diminished motor activity. In contrast to paralysis, hypokinesia is not characterized by a lack of motor strength, but rather by a poverty of movement. The typical habitual movements (e.g., folding the arms, crossing the legs) are reduced in frequency. (Human Phenotype Ontology, HP_0002375)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0002375
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Genes

11 genes associated with the hypokinesia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
AIFM1	apoptosis-inducing factor, mitochondrion-associated, 1
ATP13A2	ATPase type 13A2
GBA	glucosidase, beta, acid
GFM1	G elongation factor, mitochondrial 1
GLRA1	glycine receptor, alpha 1
LAMP2	lysosomal-associated membrane protein 2
MRPS16	mitochondrial ribosomal protein S16
MTM1	myotubularin 1
PDE8B	phosphodiesterase 8B
SLC52A2	solute carrier family 52 (riboflavin transporter), member 2
TH	tyrosine hydroxylase