F8

coagulation factor VIII
OMIM: 300841, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green F8 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.43	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Haemophilia A, MIM# 306700 MONDO:0010602 Thrombophilia 13, X-linked, due to factor VIII defect, MIM# 301071
Green F8 in Mendeliome Version 1.1902	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Haemophilia A, MIM# 306700 MONDO:0010602 Thrombophilia 13, X-linked, due to factor VIII defect, MIM# 301071
Green F8 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Mackenzie's Mission Phenotypes Hemophilia A, 306700 (3)
Green F8 in Additional findings_Paediatric Level 2: Screening Version 0.278	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources BabySeq Category A gene Expert Review Green Phenotypes Hemophilia A
Red F8 in Prepair 1000+ Level 2: Screening Version 1.9	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red Mackenzie's Mission Phenotypes Hemophilia A, 306700 (3) Tags SV/CNV
Amber F8 in BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Amber BabySeq Category A gene BeginNGS Phenotypes Haemophilia A, MIM#306700 Tags treatable haematological technically challenging
Green F8 in Transplant Co-Morbidity Superpanel Level 2: Screening Version 0.18	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Thrombophilia 13, X-linked, due to factor VIII defect, MIM# 301071 MONDO:0010602 Haemophilia A, MIM# 306700