additional crus of antihelix Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Supernumerary ridge or crus of the ear arising from the antihelix. (Human Phenotype Ontology, HP_0011235)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011235
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Genes

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

Symbol Name
SALL1 spalt-like transcription factor 1
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)