prominent crus of helix Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of an abnormally prominent of the crus of the helix (FMA:61024). That is, development of the crus helix to the same degree as an average antihelix stem or helix. (Human Phenotype Ontology, HP_0009899)
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2 genes associated with the prominent crus of 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