F9

coagulation factor IX
OMIM: 300746, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Green F9 in Inherited bleeding disorders

Level 3: Haemostasis disorders
Level 2: Haematological and immunological disorders
Version 1.182

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Other
  • Radboud University Medical Center, Nijmegen
  • Expert Review Green
  • BRIDGE Study Tier 1 Gene
Phenotypes
  • Haemophilia B
  • Thrombophilia, X-linked, due to factor IX defect 300807
Tags
  • gene-therapy-trial
Green F9 in Bleeding and platelet disorders


Level 2: Haematology
Version 4.6
Latest signed off version: v4.0 (30 Apr 2025)

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • North West GLH
  • Yorkshire and North East GLH
  • London South GLH
  • NHS GMS
  • Expert Review Green
  • Wessex and West Midlands GLH
Phenotypes
  • 306900 Haemophilia B
Green F9 in Factor IX deficiency


Level 2: Haematology
Version 1.3
Latest signed off version: v1.0 (14 Sep 2023)

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Thrombophilia, X-linked, due to factor IX defect, OMIM:300807
  • Hemophilia B, OMIM:306900
  • hemophilia B, MONDO:0010604
  • thrombophilia, X-linked, due to factor 9 defect, MONDO:0010432