F11

coagulation factor XI
OMIM: 264900, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green F11 in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.43

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Factor XI deficiency, autosomal dominant 612416
  • Factor XI deficiency, autosomal recessive, MIM#612416

Green F11 in Mendeliome


Version 1.1902

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Factor XI deficiency, autosomal dominant 612416
  • Factor XI deficiency, autosomal recessive, MIM#612416

Green F11 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 XI deficiency

Red F11 in Prepair 1000+


Level 2: Screening
Version 1.9

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Factor XI deficiency, autosomal recessive, (MIM#612416)

Red F11 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.114

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • BabySeq Category A gene
Phenotypes
  • Factor XI deficiency, autosomal dominant 612416
  • Factor XI deficiency, autosomal recessive, MIM#612416

Green F11 in Transplant Co-Morbidity Superpanel


Level 2: Screening
Version 0.18

review BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Factor XI deficiency, autosomal dominant 612416
  • Factor XI deficiency, autosomal recessive, MIM#612416