| C0015523 |
Hereditary Factor XI Deficiency |
DO |
factor XI deficiency
|
2229 |
| C0015523 |
Hereditary Factor XI Deficiency |
HPO |
Factor XI deficiency
|
HP:0001929 |
| C0015523 |
Hereditary Factor XI Deficiency |
HPO |
Reduced factor XI activity
|
HP:0001929 |
| C0015523 |
Hereditary Factor XI Deficiency |
HPO |
Low factor XI activity
|
HP:0001929 |
| C0015523 |
Hereditary Factor XI Deficiency |
ICD10 |
Hereditary factor XI deficiency
|
D68.1 |
| C0015523 |
Hereditary Factor XI Deficiency |
ICD10CM |
Hemophilia C
|
D68.1 |
| C0015523 |
Hereditary Factor XI Deficiency |
ICD10CM |
Plasma thromboplastin antecedent [PTA] deficiency
|
D68.1 |
| C0015523 |
Hereditary Factor XI Deficiency |
ICD10CM |
Hereditary factor XI deficiency
|
D68.1 |
| C0015523 |
Hereditary Factor XI Deficiency |
ICD10CM |
Rosenthal's disease
|
D68.1 |
| C0015523 |
Hereditary Factor XI Deficiency |
ICD9CM |
Congenital factor XI deficiency
|
286.2 |
| C0015523 |
Hereditary Factor XI Deficiency |
ICD9CM |
Cong factor xi disorder
|
286.2 |
| C0015523 |
Hereditary Factor XI Deficiency |
MONDO |
congenital factor XI deficiency
|
0012897 |
| C0015523 |
Hereditary Factor XI Deficiency |
MSH |
Factor XI Deficiency
|
D005173 |
| C0015523 |
Hereditary Factor XI Deficiency |
NCI |
Hemophilia C
|
C84705 |
| C0015523 |
Hereditary Factor XI Deficiency |
NCI |
Hereditary Factor XI Deficiency Disease
|
C84705 |
| C0015523 |
Hereditary Factor XI Deficiency |
NCI |
Hereditary Factor XI Deficiency
|
C84705 |
| C0015523 |
Hereditary Factor XI Deficiency |
OMIM |
FACTOR XI DEFICIENCY
|
612416 |
| C0015523 |
Hereditary Factor XI Deficiency |
ORDO |
Congenital factor XI deficiency
|
329 |