agenesis of the diaphragm Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital lack, i.e., aplasia of the diaphragm. (Human Phenotype Ontology, HP_0008986)
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1 genes associated with the agenesis of the diaphragm phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HYLS1 hydrolethalus syndrome 1