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