ISCA-37392-Loss

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green ISCA-37392-Loss Region in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.511	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert Review Phenotypes Williams-Beuren syndrome, MIM# 194050 intellectual disability growth retardation cardiovascular disease Tags SV/CNV
Green ISCA-37392-Loss Region in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.507	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert Review Phenotypes Williams-Beuren syndrome, MIM# 194050 intellectual disability growth retardation cardiovascular disease Tags SV/CNV
Green ISCA-37392-Loss Region in Common deletion and duplication syndromes Version 0.146	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Phenotypes Williams-Beuren syndrome, MIM# 194050 intellectual disability growth retardation cardiovascular disease Tags SV/CNV
Green ISCA-37392-Loss Region in Growth failure Version 1.87	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Expert Review Expert Review Phenotypes Williams-Beuren syndrome, MIM# 194050 intellectual disability growth retardation cardiovascular disease Tags SV/CNV

4 panels