Branchial Anomaly Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Congenital developmental defect arising from the primitive branchial apparatus. (Human Phenotype Ontology, HP_0009794)
External Link https://www.disgenet.org/browser/0/1/0/C1862066
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Genes

1 genes associated with the disease Branchial Anomaly in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)