VWF

von Willebrand factor
OMIM: 613160, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green VWF in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.43	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Expert Review Green Victorian Clinical Genetics Services Victorian Clinical Genetics Services Phenotypes von Willebrand disease, type 1, MIM#193400 von Willebrand disease, types 2A, 2B, 2M, and 2N, MIM#613554 von Willibrand disease, type 3, MIM#277480
Green VWF in Mendeliome Version 1.1902	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes von Willebrand disease, type 1, MIM# 193400 von Willebrand disease, type 3 , MIM#277480 von Willebrand disease, types 2A, 2B, 2M, and 2N, MIM# 613554
Green VWF in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes von Willebrand disease, types 2A, 2B, 2M, and 2N, 613554 (3)
Amber VWF in Additional findings_Paediatric Level 2: Screening Version 0.278	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Amber BabySeq Category B gene Phenotypes von Willebrand disease
Amber VWF in Prepair 1000+ Level 2: Screening Version 1.9	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber Mackenzie's Mission Phenotypes von Willebrand disease, types 2A, 2B, 2M, and 2N, 613554 (3)
Amber VWF in BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category B gene Expert Review Amber Phenotypes von Willebrand disease
Green VWF in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes von Willebrand disease, type 1, MIM#193400 von Willibrand disease, type 3, MIM#277480 von Willebrand disease, types 2A, 2B, 2M, and 2N, MIM#613554