interrupted aortic arch, type b Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Non-continuity of the aortic arch with an atretic point or absent segment between the left carotid and subclavian arteries. (Human Phenotype Ontology, HP_0011613)
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2 gene mutations causing the interrupted aortic arch, type b phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DRC1 dynein regulatory complex subunit 1
KAT6A K(lysine) acetyltransferase 6A