stahl ear Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of a supernumerary, i.e. third, crus of the helix (FMA:61024) in the helix, arising at or above the normal bifurcation of the antihelix. (Human Phenotype Ontology, HP_0100015)
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2 genes associated with the stahl ear 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)