Code
|
Display
|
68913001
|
Alpha thalassemia (disorder) |
36351005
|
Antithrombin III deficiency (disorder) |
306058006
|
Aplastic anemia (disorder) |
707147002
|
Asplenia (disorder) |
65959000
|
Beta thalassemia (disorder) |
64779008
|
Blood coagulation disorder (disorder) |
715559004
|
Combined deficiency of factor V and factor VIII (disorder) |
767712006
|
Factor IX deficiency (disorder) |
4320005
|
Factor V deficiency (disorder) |
307091009
|
Factor V Leiden mutation (disorder) |
37193007
|
Factor VII deficiency (disorder) |
76642003
|
Factor X deficiency (disorder) |
767713001
|
Factor XI deficiency (disorder) |
359727008
|
Fibrinogen deficiency (disorder) |
90935002
|
Hemophilia (disorder) |
41788008
|
Hereditary factor IX deficiency disease (disorder) |
28293008
|
Hereditary factor VIII deficiency disease (disorder) |
49762007
|
Hereditary factor XI deficiency disease (disorder) |
84828003
|
Leukopenia (disorder) |
109995007
|
Myelodysplastic syndrome (disorder) |
165517008
|
Neutropenia (finding) |
127034005
|
Pancytopenia (disorder) |
109992005
|
Polycythemia vera (disorder) |
76407009
|
Protein C deficiency disease (disorder) |
1563006
|
Protein S deficiency disease (disorder) |
440989002
|
Prothrombin G20210A mutation (disorder) |
127041004
|
Sickle cell-beta-thalassemia (disorder) |
127040003
|
Sickle cell-hemoglobin SS disease (disorder) |
417357006
|
Sickling disorder due to hemoglobin S (disorder) |
302215000
|
Thrombocytopenic disorder (disorder) |
128105004
|
von Willebrand disorder (disorder) |