C0020640 |
Inherited Factor II deficiency |
DO |
prothrombin deficiency
|
2235 |
C0020640 |
Inherited Factor II deficiency |
EFO |
thrombin
|
0003183 |
C0020640 |
Inherited Factor II deficiency |
MONDO |
congenital prothrombin deficiency
|
0013361 |
C0020640 |
Inherited Factor II deficiency |
OMIM |
PROTHROMBIN DEFICIENCY, CONGENITAL
|
613679 |
C0020640 |
Inherited Factor II deficiency |
OMIM |
HYPOPROTHROMBINEMIA
|
613679 |
C0020640 |
Inherited Factor II deficiency |
OMIM |
DYSPROTHROMBINEMIA
|
613679 |
C0020640 |
Inherited Factor II deficiency |
ORDO |
Congenital factor II deficiency
|
325 |