HEY2

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Red HEY2 in Aortopathy_Connective Tissue Disorders Level 2: Cardiovascular disorders Version 1.86	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 0.430	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 Mendeliome Version 1.2302	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 thoracic aortic aneurysms
Red HEY2 in Fetal anomalies Version 1.313	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