F10

coagulation factor X
OMIM: 613872
PanelMode of inheritanceDetails
2 panels
R-numbers: R90
Signed-off version 4.16
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
227600 Factor X deficiency
R-numbers: R119
Signed-off version 1.4
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Factor X deficiency, OMIM:227600, congenital factor X deficiency, MONDO:0009212