Stahl Ear Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
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)
External Link https://www.disgenet.org/browser/0/1/0/C1862689
Similar Terms
Downloads & Tools

Genes

2 genes associated with the disease Stahl Ear in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

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