Prominent Crus Of Helix Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link https://www.disgenet.org/browser/0/1/0/C4021377
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Genes

3 genes associated with the disease Prominent Crus Of Helix in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
TWIST1 twist family bHLH transcription factor 1