apneic episodes in infancy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Recurrent episodes of apnea occurring during infancy. (Human Phenotype Ontology, HP_0005949)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005949
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Genes

2 genes associated with the apneic episodes in infancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACADSB acyl-CoA dehydrogenase, short/branched chain
SCN4A sodium channel, voltage gated, type IV alpha subunit