F9

coagulation factor IX
OMIM: 300746, Gene2Phenotype

7 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 7 panels
Green F9 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 B, MIM# 306900 MONDO:0010604 Thrombophilia, X-linked, due to factor IX defect, MIM# 300807 MONDO:0010432
Green F9 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 B, MIM# 306900 Thrombophilia, X-linked, due to factor IX defect, MIM# 300807
Green F9 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 B, 306900 (3)
Green F9 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 B
Red F9 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 B, 306900 (3)
Green F9 in BabyScreen+ newborn screening Level 2: Screening Version 1.114	review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green BabySeq Category A gene BeginNGS Phenotypes Haemophilia B, MIM#306900 Tags treatable haematological
Green F9 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 Haemophilia B, MIM# 306900 Thrombophilia, X-linked, due to factor IX defect, MIM# 300807 MONDO:0010432 MONDO:0010604