- Agnogenic Myeloid Metaplasia (Myelofibrosis)
- Anemia, Aplastic
- Anemia, Cooley's (Beta-thalassemia)
- Anemia, Fanconi's
- Anemia, Hemolytic
- Anemia, Hypoplastic
- Anemia, Lead-Poisoning
- Anemia, Refractory
- Anemia, Sickle Cell
- Anemia, Sideroblastic
- Antithrombin III Deficiency
- Castleman's Disease
- Cold Agglutinin Disease
- Cryoglobulinemia
- Deep Vein Thrombosis (DVT)
- G6PD Deficiency
- Hand-Schueller-Christian Syndrome
- Hemochromatosis
- Hemophilia
- Hemosiderosis
- Hereditary Spherocytosis
- Histiocytoses
- Idiopathic Thrombocytopenic Purpura (ITP)
- Lymphocytopenia
- Monoclonal Gammopathy
- Myelodysplastic Syndromes
- Myelofibrosis (Agnogenic Myeloid Metaplasia)
- Osler-Weber-Rendu syndrome (Hereditary Hemorrhagic Telangiectasia)
- Polycythemia Vera; Waldenstrom's disease
- Pulmonary Embolism
- Pure Red Cell Aplasia; Erythroblastopenia
- Rh Incompatibility
- Thalassemia
- Thrombasthenia (Congenital platelet function defects)
- Thrombocythemia. Primary
- Thrombophlebitis (Superficial vein thrombophlebitis)
- Von Willebrand Disease
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