Atrioventricular septal defect, susceptibility to, 2
MONDO:0011650Any atrioventricular septal defect in which the cause of the disease is a mutation in the CRELD1 gene.
Also known as: CRELD1 atrioventricular septal defect, atrioventricular septal defect caused by mutation in CRELD1, atrioventricular septal defect, susceptibility to, 2, atrioventricular septal defect, susceptibility to, type 2, AVSD2, atrioventricular septal defect, partial, with heterotaxy syndrome, susceptibility to atrioventricular septal defect 2
0 clinical trials for this condition and its sub-types, 0 tagged with Atrioventricular septal defect, susceptibility to, 2 itself.
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