pectus excavatum of inferior sternum Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Pectus excavatum (defect of the chest wall characterized by depression of the sternum) affecting primarily the inferior region of the sternum. (Human Phenotype Ontology, HP_0000915)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000915
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Genes

3 genes associated with the pectus excavatum of inferior sternum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NF1 neurofibromin 1
PTPN11 protein tyrosine phosphatase, non-receptor type 11
SOS1 son of sevenless homolog 1 (Drosophila)