infantile axial hypotonia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Muscular hypotonia (abnormally low muscle tone) affecting the musculature of the trunk and with onset in infancy. (Human Phenotype Ontology, HP_0009062)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009062
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Genes

1 genes associated with the infantile axial hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HSD17B10 hydroxysteroid (17-beta) dehydrogenase 10