Disease #00916 (AVSD3 (septal defect, atrioventricular, type 3 (AVSD-3)), OMIM:600309)

Official abbreviation AVSD3
Name septal defect, atrioventricular, type 3 (AVSD-3)
OMIM ID 600309
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene GJA1
Associated tissues -
Disease features -
Remarks -