F12

coagulation factor XII
OMIM: 610619, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green F12 in COVID-19 research Level 2: Viral research Version 1.141	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 1.177	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 Version 4.201 Latest signed off version: v4.0 (22 Mar 2023)	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 Version 1.63 Latest signed off version: v1.3 (15 Oct 2020)	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 Version 3.9 Latest signed off version: v3.0 (22 Mar 2023)	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
Green F12 in Severe Paediatric Disorders Version 1.184	review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Next Generation Children Project Expert Review Green Expert list Phenotypes Angioedema, hereditary, 3, OMIM:610618 Factor XII deficiency, OMIM:234000