Diseases Treated.

Full List of FDA-Approved Cord Blood Treatments

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  • LEUKEMIAS, LYMPHOMAS and BONE MARROW CANCERS: Cancers of the blood cells that make up the immune system.
    • Acute Lymphoblastic/Lympocytic Leukemia (ALL)
    • Acute Myelogenous Leukemia (AML)
    • Acute Biphenotypic Leukemia
    • Acute Undifferentiated Leukemia
    • Adult T-cell Leukemia/Lymphoma
    • Chronic Lymphocytic Leukemia (CLL)
    • Chronic Myelogenous Leukemia (CML)
    • Chronic Myelomonocytic Leukemia (CMML)
    • Hodgkin’s Lymphoma
    • Juvenile Chronic Myelogenous Leukemia (JCML)
    • Juvenile Myelomonocytic Leukemia (JMML)
    • Multiple Myeloma
    • Myelodysplastic Syndrome
    • Myeloid/Natural Killer (NK) Cell Precursor Acute Leukemia
    • Non-Hodgkin’s Lymphoma
    • Plasma Cell Leukemia
    • Prolymphocytic Leukemia
    • Refractory Anemia (RA)
    • Refractory Anemia with Ringed Sideroblasts (RARS)
    • Refractory Anemia with Excess Blasts (RAEB)
    • Refractory Anemia with Excess Blasts in Transformation (RAEB-T)
    • Waldenstrom’s Macroglobulinemia
  • SOLID TUMORS: Cancers of cells from organs of the body.
    • Ewing Sarcoma
    • Medulloblastoma
    • Nephroblastoma (Wilms Tumor)
    • Neuroblastoma
    • Retinoblastoma
    • Rhabdomyosarcoma
    • Thymoma (Thymic Carcinoma)

  • ANEMIAS: Diseases causing too few blood cells to be made.
    • Aplastic Anemia (Severe)
    • Congenital Cytopenia
    • Congenital Dyserythropoietic Anemia
    • Fanconi Anemia
    • Paroxysmal Nocturnal Hemoglobinuria (PNH)

  • INHERITED RED CELL ABNORMALITIES: Genetic diseases resulting in red blood cells that do not work correctly.
    • Beta Thalassemia Major (also known as Cooley’s Anemia)
    • Blackfan-Diamond Anemia
    • Pure Red Cell Aplasia
    • Sickle Cell Disease
  • INHERITED PLATELET ABNORMALITIES: Genetic diseases resulting in platelets that are not able to correctly form clots.
    • Amegakaryocytosis / Congenital Thrombocytopenia
    • Glanzmann Thrombasthenia
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  • IMMUNE SYSTEM DISORDERS: Genetic or acquired diseases which result in white blood cells that are not able to fight off infections.
    • Acute Myelofibrosis
    • Agnogenic Myeloid Metaplasia (Myelofibrosis)
    • Ataxia-Telangiectasia
    • Bare Lymphocyte Syndrome
    • Cartilage-Hair Hypoplasia
    • Chediak-Higashi Syndrome
    • Chronic Active Epstein Barr Virus
    • Chronic Granulomatous Disease
    • Common Variable Immunodeficiency
    • Congenital Neutropenia
    • DiGeorge Syndrome
    • Dyskeratosis Congenita
    • Essential Thrombocythemia
    • Evans Syndrome
    • Gunther’s Disease (Congenital Erythropoietic Porphyria)
    • IKK Gamma Deficiency (NEMO Deficiency)
    • Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) Syndrome
    • Hemophagocytic Lymphohistiocytosis (HLH)
    • Hermansky-Pudlak Syndrome
    • Kostmann Syndrome
    • Langerhans Cell Histiocytosis (Histiocytosis X)
    • Leukocyte Adhesion Deficiency
    • Lymphoproliferative Disorders (LPD)
    • Lymphoproliferative Disorder, X-linked (also known as Epstein-Barr Virus Susceptibility)
    • Myelokathexis
    • Myeloproliferative Disorders
    • Neutrophil Actin Deficiency
    • Omenn Syndrome (SCID)
    • Pearson’s Syndrome
    • Polycythemia Vera
    • Reticular Dysgenesis (SCID)
    • SCID with Adenosine Deaminase Deficiency (ADA-SCID)
    • SCID with absence of T & B Cells
    • SCID with absence of T cells, Normal B Cells
    • SCID with Purine Nucleoside Phosphorylase Deficiency
    • SCID which is X-linked
    • Shwachman-Diamond Syndrome
    • Systemic Amyloidosis
    • Systemic Mastocytosis
    • Thymic dysplasia
    • Wiskott-Aldrich Syndrome
    • X-linked Agammaglobulinemia
    • X-linked Hyper-IgM Syndrome
    • X-linked Lymphoproliferative Disorder
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  • INHERITED METABOLIC DISORDERS: Genetic diseases that prevent the body from correctly processing normal substances in the body or diet.
    • Adrenoleukodystrophy (ALD)/Adrenomyeloneuropathy (AMN)
    • Fucosidosis
    • Gaucher Disease
    • Hunter’s Syndrome (MPS-II)
    • Hurler’s Syndrome (MPS-IH)
    • Krabbe Disease (Globoid Cell Leukodystrophy)
    • Lesch-Nyhan Syndrom
    • Mannosidosis
    • Maroteaux-Lamy Syndrome (MPS-VI)
    • Metachromatic Leukodystrophy
    • Morquio Syndrome (MPS-IV)
    • Mucolipidosis II (I-cell Disease)
    • Mucopolysaccharidoses (MPS)
    • Niemann-Pick Disease
    • Neruonal Ceroid Liopfuscinosis (Batten Disease)
    • Osteopetrosis
    • Pelizaeus-Merzbacher Disease
    • Sandhoff Disease
    • Sanfilippo Syndrome (MPS-III)
    • Scheie Syndrome (MPS-IS)
    • Sly Syndrome, Beta-Glucuronidase Deficiency (MPS-VII)
    • Tay-Sachs Disease
    • Wolman Disease
    • X-linked Adrenoleukodystrophy
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