choanal stenosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal narrowing of the choana (the posterior nasal aperture). (Human Phenotype Ontology, HP_0000452)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000452
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Genes

15 genes associated with the choanal stenosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FAM20C family with sequence similarity 20, member C
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FRAS1 Fraser extracellular matrix complex subunit 1
FREM2 FRAS1 related extracellular matrix protein 2
GRIP1 glutamate receptor interacting protein 1
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
POLR1D polymerase (RNA) I polypeptide D, 16kDa
POR P450 (cytochrome) oxidoreductase
PTDSS1 phosphatidylserine synthase 1
PTH1R parathyroid hormone 1 receptor
RECQL4 RecQ protein-like 4
SALL4 spalt-like transcription factor 4
SETBP1 SET binding protein 1
SOST sclerostin