F12

coagulation factor XII
OMIM: 610619, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels
Green F12 in COVID-19 research


Level 2: Viral research
Version 1.146

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • London North GLH
  • NHS GMS
  • GRID V2.0
  • North West GLH
  • Victorian Clinical Genetics Services
  • Expert Review Green
  • NHS GMS
  • North West GLH
  • London North GLH
  • Expert Review Green
  • Victorian Clinical Genetics Services
  • GRID V2.0
Phenotypes
  • Angioedema, hereditary, 3, OMIM:610618
Green F12 in Inherited bleeding disorders

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

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • BRIDGE Study Tier 1 Gene
Phenotypes
  • Angioedema, hereditary, type III, OMIM:610618
  • Factor XII deficiency, OMIM:234000
Tags
  • watchlist_moi
Green F12 in Primary immunodeficiency or monogenic inflammatory bowel disease


Level 2: Immunology
Version 8.78
Latest signed off version: v8.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • NHS GMS
  • North West GLH
  • London North GLH
  • Expert Review Green
  • Victorian Clinical Genetics Services
  • GRID V2.0
Phenotypes
  • Angioedema, hereditary, 3, OMIM:610618
Green F12 in Vascular skin disorders


Level 2: Dermatology
Version 2.5
Latest signed off version: v2.0 (30 Apr 2025)

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • London North GLH
  • NHS GMS
  • Expert Review Green
Phenotypes
  • Angioedema, hereditary, type III, OMIM:610618
  • Factor XII deficiency, OMIM:234000
Green F12 in Bleeding and platelet disorders


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

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • North West GLH
  • Yorkshire and North East GLH
  • London South GLH
  • NHS GMS
  • Expert Review Green
  • Wessex and West Midlands GLH
Phenotypes
  • Angioedema, hereditary, type III, OMIM:610618
  • Factor XII deficiency, OMIM:234000