Leukemias
(60,000 Diagnoses Each Year) |
Acute Lymphoblastic Leukemia |
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Acute Myelogenous Leukemia |
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Acute Biphenotypic Leukemia |
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Acute Undifferentiated Leukemia |
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Acute Lymphoblastic Leukemia |
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Acute Myelogenous Leukemia (AML) |
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Chronic Lymphocytic Leukemia (CLL) |
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Juvenile Chronic Myelogenous Leukemia (JCML) |
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Juvenile Myelomonocytic Leukemia (JMML) |
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Refractory Anemia (RA) |
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Refractory Anemia with Ringed Sideroblasts (RARS) |
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Refractory Anemia with Excess Blasts (RAEB) |
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Refractory Anemia with Excess Blasts in Transformation (RAEB-T) |
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Chronic Myelomonocytic Leukemia (CMML) |
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Lymphomas
(80,000 Diagnoses Each Year) |
Hodgkin’s Lymphoma |
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Solid Tumors |
Neuroblastoma |
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Medulloblastoma |
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Retinoblastoma |
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Anemias |
Aplastic Anemia |
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Congenital Dyserythropoietic Anemia |
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Fanconi Anemia |
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Paroxysmal Nocturnal Hemoglobinuria (PNH) |
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Inherited Red Cell Abnormalities |
Beta Thalassemia Major (also known as Cooley’s Anemia) |
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Blackfan-Diamond Anemia |
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Pure Red Cell Aplasia |
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Sickle Cell Disease |
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Inherited Platelet Abnormalities |
Amegakaryocytosis / Congenital Thrombocytopenia |
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Glanzmann Thrombasthenia |
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Inherited Immune System Disorders |
SCID with Adenosine Deaminase Deficiency (ADA-SCID) |
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SCID which is X-linked |
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SCID with absence of T & B Cells |
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SCID with absence of T Cells, Normal B Cells |
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Omenn Syndrome |
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Kostmann Syndrome |
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Ataxia–Telangiectasia |
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Bare Lymphocyte Syndrome |
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Common Variable Immunodeficiency |
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DiGeorge Syndrome |
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Leukocyte Adhesion Deficiency |
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Lymphoproliferative Disorders (LPD) |
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Lymphoproliferative Disorder, X-linked (also known as Epstein–Barr Virus Susceptibility) |
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Wiskott–Aldrich Syndrome |
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Myeloproliferative Disorders |
Acute Myelofibrosis |
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Agnogenic Myeloid Metaplasia (Myelofibrosis) |
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Polycythemia Vera |
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Essential Thrombocythemia |
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Phagocyte Disorders |
Chediak–Higashi Syndrome |
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Chronic Granulomatous Disease |
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Neutrophil Actin Deficiency |
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Reticular Dysgenesis |
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Bone Marrow Cancers |
Multiple Myeloma |
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Plasma Cell Leukemia |
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Waldenstrom’s Macroglobulinemia |
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Inherited Immune & Other System Disorders |
Cartilage–Hair Hypoplasia |
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Gunther’s Disease (Erythropoietic Porphyria) |
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Hermansky–Pudlak Syndrome |
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Pearson’s Syndrome |
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Shwachman–Diamond Syndrome |
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Systemic Mastocytosis |
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Inherited Metabolic Disorders |
Mucopolysaccharidoses (MPS) |
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Hurler’s Syndrome (MPS–IH) |
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Scheie Syndrome (MPS–IS) |
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Hunter’s Syndrome (MPS–II) |
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Sanfilippo Syndrome (MPS–III) |
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Morquio Syndrome (MPS–IV) |
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Maroteaux–Lamy Syndrome (MPS–VI) |
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Sly Syndrome, Beta–Glucuronidase Deficiency (MPS–VII) |
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Mucolipidosis II (I–cell Disease) |
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Adrenoleukodystrophy (ALD)/Adrenomyeloneuropathy (AMN) |
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Krabbe Disease (Globoid Cell Leukodystrophy) |
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Metachromatic Leukodystrophy |
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Pelizaeus–Merzbacher Disease |
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Gaucher Disease |
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Niemann–Pick Disease |
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Sandhoff Disease |
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Tay–Sachs Disease |
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Wolman Disease |
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Lesch–Nyhan Syndrome |
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Osteopetrosis |
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