abnormal branching pattern of the aortic arch Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A deviance from the norm of the origin or course of the right brachiocephalic artery, the left common carotid artery, the left subclavian artery or the proximal vertebral arteries. (Human Phenotype Ontology, HP_0011587)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011587
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6 genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACVR2B activin A receptor, type IIB
CREBBP CREB binding protein
CRELD1 cysteine-rich with EGF-like domains 1
PIK3R2 phosphoinositide-3-kinase, regulatory subunit 2 (beta)
STRA6 stimulated by retinoic acid 6
TBX1 T-box 1