F11

coagulation factor XI
OMIM: 264900, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green F11 in Bleeding and Platelet Disorders Level 2: Haematological disorders Version 1.62	2 reviews	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 1.3512	1 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	0 reviews	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 2.14	2 reviews	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 Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	1 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 Level 2: Screening Version 0.20	0 reviews	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