MCFD2

multiple coagulation factor deficiency 2
OMIM: 607788, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green MCFD2 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.43	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Factor V and factor VIII, combined deficiency of, MIM# 613625 MONDO:0013331
Green MCFD2 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Factor V and factor VIII, combined deficiency of, MIM# 613625 MONDO:0013331
Green MCFD2 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 Factor V and factor VIII, combined deficiency of, 613625 (3)
Green MCFD2 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Factor V and Factor VIII deficiency, combined
Green MCFD2 in Prepair 1000+ Level 2: Screening Version 1.9	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Factor V and factor VIII, combined deficiency of, 613625 (3)
Amber MCFD2 in BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Amber BabySeq Category A gene Phenotypes Factor V and factor VIII, combined deficiency of, MIM# 613625 Tags treatable haematological
Green MCFD2 in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Factor V and factor VIII, combined deficiency of, MIM# 613625 MONDO:0013331