TBX2

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Amber TBX2 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.430	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert list Phenotypes Vertebral anomalies and variable endocrine and T-cell dysfunction, MIM# 618223
Amber TBX2 in Mendeliome Version 1.2302	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Victorian Clinical Genetics Services Phenotypes Vertebral anomalies and variable endocrine and T-cell dysfunction - MIM#618223
Red TBX2 in Clefting disorders Level 3: Dysmorphic disorders Level 2: Dysmorphic and congenital abnormality syndromes Version 0.260	1 review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Red Expert list Phenotypes Vertebral anomalies and variable endocrine and T-cell dysfunction, MIM# 618223
Amber TBX2 in Fetal anomalies Version 1.313	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber Expert list Literature Phenotypes Vertebral anomalies and variable endocrine and T-cell dysfunction - MIM#618223 Congenital heart disease skeletal abnormalities thymus aplasia

4 panels