HEY2

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Red HEY2 in Aortopathy_Connective Tissue Disorders Level 2: Cardiovascular disorders Version 1.100	1 review	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes congenital heart defects and thoracic aortic aneurysms
Red HEY2 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.474	2 reviews	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Congenital heart disease, MONDO:0005453, HEY2-related
Red HEY2 in Mendeliome Version 1.3512	1 review	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Congenital heart disease, MONDO:0005453, HEY2-related thoracic aortic aneurysms
Red HEY2 in Fetal anomalies Version 1.465	1 review	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes congenital heart defects and thoracic aortic aneurysms

4 panels