abnormality of the crus of the helix Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the crus of the helix (FMA:61024), which is the horizontal piece of cartilage located outside the ear canal that divides the upper and lower parts of the ear. (Human Phenotype Ontology, HP_0009895)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009895
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Genes

2 genes associated with the abnormality of the crus of the helix phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FGFR2 fibroblast growth factor receptor 2
TWIST1 twist family bHLH transcription factor 1