laryngeal hypoplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the larynx (FMA:55097). (Human Phenotype Ontology, HP_0008749)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008749
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Genes

3 genes associated with the laryngeal hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
HYLS1 hydrolethalus syndrome 1
PRRX1 paired related homeobox 1
SF3B4 splicing factor 3b, subunit 4, 49kDa