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
Subcategories
This category has the following 6 subcategories, out of 6 total.
A
C
H
R
S
Pages in category "Blood disorders"
The following 200 pages are in this category, out of 278 total.
(previous page) (next page)A
- Acquired hemolytic anemia
- Acute lymphoid leukemia
- Acute monoblastic and monocytic leukemia
- Acute posthemorrhagic anemia
- Advate
- Algaemia
- Alimentary toxic aleukia
- Alloimmune
- Alpha thalassemia
- Alpha-thalassemia
- AML
- Anaemia
- Analbuminemia
- Andexxa
- Anemia of prematurity
- Anemias
- Anemic hypoxia
- Anisochromia
- Anti-phospholipid antibody
- Anti-thrombin antibodies
- Anticardiolipin antibodies
- Apadamtase alfa
- Aplasia
- Aplastic anaemia
- Aplastic anemia
- ATR-X syndrome
B
- B-cell leukemia
- Bacteremia
- Bandemia
- Basopenia
- Basophilia
- Basophilic stippling
- Bisalbuminemia
- Bleeding diathesis
- Bleeding disorder
- Bleeding problems
- Blood cancer
- Blood cancers
- Blood clotting disorders
- Blood coagulation disorders
- Blood disorder
- Blood disorders
- Blood dyscrasia
- Blood-borne disease
- Blooded
- Bloodstream infections
- Bone marrow failure
C
- Capillary leak syndrome with monoclonal gammopathy
- Carcinocythemia
- Ceprotin
- Cerebral thrombosis
- Cerebral venous sinus thrombosis
- Cerebral venous thrombosis
- Childhood myelodysplastic syndrome
- Christmas disease
- Coagadex
- Coagulation disorder
- Coagulation factor deficiency
- Coagulopathies
- Coagulopathy
- COAT platelet defect
- Cold autoimmune hemolytic anemia
- Congealing
- Congenital afibrinogenemia
- Congenital antithrombin III deficiency
- Congenital dyserythropoietic anemia
- Congenital hypofibrinogenemia
- Congenital spherocytic anemia
- Corifact
- Cryofibrinogenemia
- Cyclic neutropenia
- Cystic fibrosis gastritis megaloblastic anemia
- Cytopenia
D
E
F
H
- Haemo
- Haemolysin
- Haemolytic anaemia
- Haemophilia A
- Haemophilia B
- Haemophilia C
- Haemorrhagic
- Hairy cell leukemia
- Heinz mean
- Hematologic disease
- Hematologic disorder
- Hematological disorder
- Heme arginate
- Hemoconcentration
- Hemoglobin Barts
- Hemoglobin c disease
- Hemoglobin C disease
- Hemoglobin decreased
- 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
- Hemolytic uremic syndrome, atypical, childhood
- Hemolytic-uremic syndrome
- Hemophilia a
- Hemorrhagic cyst
- Hemorrhagic thrombocythemia
- Hepatic veno-occlusive disease
- Veno-occlusive disease
- Hepatitis G virus
- Hereditary elliptocytosis 2, 3
- Hereditary hemochromatosis
- Hereditary macrothrombocytopenia
- Hereditary pyropoikilocytosis
- High molecular weight kininogen deficiency
- Hydremia
- Hyperalbuminemia
- Hyperbilirubinemia
- Hypercalcaemia
- Hyperproteinemia
- Hyperprothrombinemia
- Hypersegmented neutrophil
- Hypoalbuminemia
- Hypocholesterolemia
- Hypochromic anemia
- Hypogammaglobulinemia
- Hypoproconvertinemia
- Hypoproteinemia
I
L
M
- Macrocytic anemia
- Macroglobulinemia
- Management of thalassemia
- Mast cell disease
- McLeod
- McLeod syndrome
- MDS
- Mediterranean anemia
- Methaemalbuminaemia
- Methemoglobinemia
- Microangiopathic hemolytic anemia
- Microcytosis
- Monoblastic leukemia
- Monoclonal gammopathy of undetermined significance
- Monocytic leukemia
- Monocytopenia
