F12

coagulation factor XII
OMIM: 610619
PanelMode of inheritanceDetails
3 panels
R-numbers: R90
Signed-off version 3.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Angioedema, hereditary, type III, OMIM:610618, Factor XII deficiency, OMIM:234000
R-numbers: R15
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Angioedema, hereditary, 3, OMIM:610618
R-numbers: R326
Signed-off version 1.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Hereditary angioedema