underdeveloped antitragus Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduction in the anterosuperior prominence of the area between the bottom of the incisura and the inner margin of the antihelix. (Human Phenotype Ontology, HP_0011251)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011251
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1 genes associated with the underdeveloped antitragus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KCTD1 potassium channel tetramerization domain containing 1