În continuare vedeţi lista de afecţiuni tratate cu unitati din sângele cordonului ombilical ale New York Blood Center (NYBC), în cadrul National Cord Blood Program- USA:
| DIAGNOSIS for Transplantation with NYBC CB units | Patients |
|---|---|
| Leukemias | 2030 |
| Acute Lymphoblastic Leukemia | 851 |
| Acute Myelogenous Leukemia | 859 |
| Acute Biphenotypic Leukemia | 29 |
| Chronic Lymphocytic Leukemia | 27 |
| Chronic Myelogenous Leukemia | 203 |
| Chronic Myelomonocytic Leukemia | 1 |
| Juvenile Chronic Myelogenous Leukemia | 34 |
| Juvenile Mono-myelocytic Leukemia | 23 |
| Leukemia, unspecified | 3 |
| Lymphomas | 201 |
| Non-Hodgkin’s Lymphoma | 121 |
| Hodgkin’s Disease | 61 |
| Epstein-Barr Virus / Lymphoproliferative Disease | 2 |
| Autoimmune Lymphoproliferative Disease | 1 |
| Lymphoma, unspecified | 16 |
| Myelodysplasias | 186 |
| Myelodysplastic Syndrome | 178 |
| Myelofibrosis | 8 |
| Bone Marrow Failure Syndromes | 236 |
| Amegakaryocytic Thrombocytopenia | 11 |
| Diamond-Bleackfan Anemia | 16 |
| Dyskeratosis Congenita | 7 |
| Fanconi’s Anemia | 95 |
| Parxysmal Nocturnal Hemoglobinuria | 2 |
| Reticular Dysgenesis | 1 |
| Severe Aplastic Anemia, unspecified | 98 |
| Shwachman-Diamond Syndrome | 5 |
| Sideroblastic Anemia | 1 |
| Hemoglobinopathies | 49 |
| Sickle Cell Disease | 20 |
| Thalassemia | 29 |
| Immune Deficiencies | 201 |
| Common Variable Immune Deficiency | 2 |
| Congenital Immune Deficiency | 1 |
| DiGeorge Syndrome | 1 |
| Griscelli Syndrome | 3 |
| Lymphocyte Adhesion Disease | 10 |
| Nezelof Syndrome | 1 |
| Omenn Syndrome | 7 |
| Severe Combined Immune Deficiency (SCID) | 113 |
| Wiskott-Aldrich Syndrome | 55 |
| X-linked Hyper-IgM Syndrome | 6 |
| X-linked Immune Dysregulation Polyendocrine Enteropathy | 2 |
| Histiocytosis | 82 |
| Familial Erythrophagocytic Lymphohistiocytosis | 24 |
| Hemophagocytic Lymphohistiocytosis | 50 |
| Hemophagocytic Syndrome | 1 |
| Histiocytosis | 2 |
| Langerhans Cell Histiocytosis (Histiocytosis-X) | 1 |
| X-Linked Lymphoproliferative Disease | 4 |
| Metabolic/Storage Diseases | 213 |
| MPS, not specified | 1 |
| Hurler Disease (MOS type IH) | 49 |
| Hurler-Scheie Disease (MPS type IS) | 2 |
| Hunter’s Syndrome (MPS type II) | 5 |
| Sanfilippo Disease (MPS type III) | 2 |
| Morquio Syndrome (MPS type IV) | 1 |
| Maroteaux-Lamy Syndrome (MPS type VI) | 9 |
| Adrenoleukodystrophy | 34 |
| Alpha-mannosidosis | 3 |
| Amyloidosis | 1 |
| Aspartylglucosaminuria | 1 |
| Austin’s Disease (Multiple Sulfatase Deficiency) | 1 |
| Fucosidosis | 1 |
| Gangliosidosis | 1 |
| Gaucher’s Disease | 2 |
| I-cell Disease (Inclusion Cell Disease) | 4 |
| Infantile Ceroid Lipofucoscinosis | 1 |
| Krabbe Disease | 22 |
| Lesch-Nyhan Syndrome | 4 |
| Metachromatic Leukodystrophy | 18 |
| Neiman-Pick Disease | 1 |
| Osteopetrosis | 42 |
| Sandhoff Disease | 1 |
| Sialidosis | 1 |
| Tay Sach Disease | 3 |
| Wolman Disease | 3 |
| Neutrophil Disorders | 27 |
| Chediak-Higashi Syndrome | 6 |
| Chronic Granulomatous Disease (CGD) | 10 |
| Congenital Neutropenia | 1 |
| Kostmann Syndrome | 10 |
| Platelet Disorders | 4 |
| Congenital Thrombocytopenia | 1 |
| Glanzmann’s Thrombasthenia | 3 |
| Other Malignancies | 29 |
| Breast Cancer | 1 |
| Multiple Myeloma (Plasma Cell Disorder) | 12 |
| Neuroblastoma | 15 |
| Other Malignancy | 1 |
| Autoimmune diseases | 1 |
| Systemic Lupus (SLE) | 1 |
| Porphyria | 1 |
| Congenital Erythropoietic Porphyria | 1 |
| Other | 1 |
| Epidermolysis Bullosa | 1 |