Category:Blood disorders
From WikiMD.com Medical Encyclopedia
 | This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes D50-D89 should be included in this category. |
For more information see the articles hematology and blood diseases
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Subcategories
This category has the following 6 subcategories, out of 6 total.
A
C
H
R
S
Pages in category "Blood disorders"
The following 162 pages are in this category, out of 162 total.
A
B
C
D
H
- Haemo
- Haemophilia A
- Haemophilia B
- Haemophilia C
- Hairy cell leukemia
- Heinz mean
- Hematologic disease
- Heme arginate
- Hemoglobin Barts
- Hemoglobin E
- Hemoglobin H disease
- Hemoglobin Lepore syndrome
- Hemoglobin M disease
- Hemoglobin O
- Hemoglobin, alpha 2
- Hemoglobinemia
- Hemolytic anemia
- Hemolytic anemia lethal genital anomalies
- Hemolytic uremic syndrome, atypical, childhood
- Hepatic veno-occlusive disease
- Hereditary pyropoikilocytosis
- High molecular weight kininogen deficiency
- Hyperbilirubinemia in adults
- Hypercalcaemia
- Hyperproteinemia
- Hyperprothrombinemia
- Hypersegmented neutrophil
- Hypoalbuminemia
- Hypocholesterolemia
- Hypochromic anemia
- Hypogammaglobulinemia
- Hypoproteinemia
L
M
- Macrocytic anemia
- Macroglobulinemia
- McLeod
- McLeod syndrome
- MDS
- Methaemalbuminaemia
- Methemoglobinemia
- Microangiopathic hemolytic anemia
- Microcytosis
- Monoclonal gammopathy of undetermined significance
- Monocytic leukemia
- Monocytopenia
- Monocytosis
- Myelodysplastic–myeloproliferative diseases
- Myelophthisic anemia
- Myeloproliferative neoplasm
N
P
- Paroxysmal hemoglobinuria
- Poikiloblast
- Poikilocytosis
- Poikiloderma with neutropenia
- Polychromasia
- Polycythemia
- Polycythemia vera
- Portal vein thrombosis
- Prefibrotic primary myelofibrosis
- Primary fibrinogenolysis
- Prolymphocytic leukemia
- Protein R deficiency
- Prothrombin G20210A
- Pseudo gray platelet syndrome
- Pyknocytosis
S
T
- Thrombomodulin anomalies, familial
- Thrombophilia
- Thrombotic microangiopathy
- Thrombotic thrombocytopenic purpura
- Tinzaparin sodium
- Toxemia
- Transfusion hemosiderosis
- Transfusion therapy (Sickle-cell disease)
- Transfusion-dependent anemia
- Transient myeloproliferative disease
- Traumatic purpura
- TTP
- Tulip fingers
