central hypotonia Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Reduced muscle tone secondary to an abnormality of the central nervous system. (Human Phenotype Ontology, HP_0011398)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0011398
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Genes

7 genes associated with the central hypotonia 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
KDM6A	lysine (K)-specific demethylase 6A
PEX13	peroxisomal biogenesis factor 13
PEX14	peroxisomal biogenesis factor 14
PEX19	peroxisomal biogenesis factor 19
PIGA	phosphatidylinositol glycan anchor biosynthesis, class A
ST3GAL3	ST3 beta-galactoside alpha-2,3-sialyltransferase 3