generalized neonatal hypotonia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Muscular hypotonia (abnormally low muscle tone) manifesting in the neonatal period and affecting the entire musculature. (Human Phenotype Ontology, HP_0008935)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008935
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Genes

7 genes associated with the generalized neonatal hypotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PEX10 peroxisomal biogenesis factor 10
PEX12 peroxisomal biogenesis factor 12
PEX16 peroxisomal biogenesis factor 16
PEX2 peroxisomal biogenesis factor 2
PEX26 peroxisomal biogenesis factor 26
PEX3 peroxisomal biogenesis factor 3
PEX6 peroxisomal biogenesis factor 6