Any congenital hypothyroidism in dogs in which the cause of the disease is a mutation in the SCL5AG gene.
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Phelan-McDermid syndrome, non-human animal
MONDO:1010006
atrial septal defect, non-human animal
MONDO:1010009
patent ductus arteriosus, non-human animal
MONDO:1010017
supravalvular aortic stenosis, non-human animal
MONDO:1010020
tetralogy of fallot, non-human animal
MONDO:1010021
ventricular septal defect, non-human animal
MONDO:1010022