aplasia/hypoplasia of the diaphragm Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Absence or underdevelopment of the diaphragm. (Human Phenotype Ontology, HP_0010315)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0010315
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Genes

1 genes associated with the aplasia/hypoplasia 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