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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008986
Similar Terms
Downloads & Tools

Genes

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