laryngeal atresia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Congenital absence of the lumen of the larynx. (Human Phenotype Ontology, HP_0008750)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008750
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Genes

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

Symbol Name
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1