Diseases treated with Cord Blood
Cord Blood contains Hematopoietic stem cells (HSCs) that have been officially approved by the FDA for use in regenerative medicine. This exciting development brings optimism for the potential treatment of a wide range of blood related disorders.
Cancer
Blood Disorders
Metabolic Disorders
Immune Disorders
Cancer
- Acute Biphenotypic Leukemia
- Acute Lymphocytic Leukemia (ALL)
- Acute Myelogenous Leukemia (AML)
- Acute Undifferentiated Leukemia
- Adult T Cell Leukemia/Lymphoma
- Chronic Active Epstein Barr
- Chronic Lymphocytic Leukemia (CLL)
- Chronic Myelogenous Leukemia (CML)
- Chronic Myelomonocytic Leukemia (CMML)
- Ewing Sarcoma
- Hodgkin’s Lymphoma
- Juvenile Chronic Myelogenous Leukemia (JCML)
- Juvenile Myelomonocytic Leukemia (JMML)
- Myeloid/Natural Killer (NK) Cell
- PrecursorAcute Leukemia
- Non-Hodgkin’s Lymphoma
- Prolymphocytic Leukemia
- Plasma Cell Leukemia
- Leukocyte Adhesion Deficiency
- Multiple Myeloma
- Neuroblastoma
- Rhabdomyosarcoma
- Thymoma (Thymic Carcinoma)
- Waldenstrom’s Macroglobulinemia
- Wilms Tumor
Blood Disorders
- Acute Myelofibrosis
- Agnogenic Myeloid Metaplasia (Myelofibrosis)
- Amyloidosis
- Aplastic Anemia (Severe)
- Beta Thalassemia Major
- Blackfan-Diamond Anemia
- Congenital Amegakaryocytic Thrombocytopenia (CAT)
- Congenital Cytopenia
- Congenital Dyserythropoietic Anemia
- Dyskeratosis Congenita
- Essential Thrombocythemia
- Fanconi Anemia
- Glanzmann’s Thrombasthenia
- Myelodysplastic Syndrome
- Paroxysmal Nocturnal Hemoglobinuria (PNH)
- Polycythemia Vera
- Pure Red Cell Aplasia
- Refractory Anemia with Excess Blasts (RAEB)
- Refractory Anemia with Excess Blasts in Transition (RAEB-T)
- Refractory Anemia with Ringed Sideroblasts (RARS)
- Shwachman-Diamond Syndrome
- Sickle Cell Disease
Metabolic Disorders
- Congenital Erythropoietic Porphyria (Gunther Disease)
- Gaucher Disease
- Hunter Syndrome (MPS-II)
- Hurler Syndrome (MPS-IH)
- Krabbe Disease
- Lesch-Nyhan Syndrome
- Mannosidosis
- Maroteaux-Lamy Syndrome (MPS-VI)
- Metachromatic Leukodystrophy
- Mucolipidosis II (I-cell Disease)
- Neuronal Ceroid Lipofuscinosis (Batten Disease)
- Niemann-Pick Disease
- Sandhoff Disease
- Sanfilippo Syndrome (MPS-III)
- Scheie Syndrome (MPS-IS)
- Sly Syndrome (MPS-VII)
- Tay Sachs
- Wolman Disease
- X-Linked Adrenoleukodystrophy
Immune Disorders
- Adenosine Deaminase Deficiency (SCID)
- Bare Lymphocyte Syndrome (SCID)
- Chediak-Higashi Syndrome (SCID)
- Chronic Granulomatous Disease
- Congenital Neutropenia
- DiGeorge Syndrome
- Evans Syndrome
- Fucosidosis
- Hemophagocytic Lymphohistiocytosis (HLH)
- Hemophagocytosis Langerhans’ Cell
Histiocytosis (Histiocytosis X) - IKK Gamma Deficiency (NEMO Deficiency)
- Immune Dysregulation, Polyendocrinopathy,
Enteropathy, X-linked (IPEX) Syndrome
- Kostmann Syndrome (SCID)
- Myelokathexis
- Omenn Syndrome (SCID)
- Phosphorylase Deficiency (SCID)
- Purine Nucleoside (SCID)
- Reticular Dysgenesis (SCID)
- Severe Combined Immunodeficiency Diseases (SCID)
- Thymic Dysplasia
- Wiskott-Aldrich Syndrome
- X-linked Agammaglobulinemia
- X-Linked Hyper IgM Syndrome
- X-Linked Lymphoproliferative Disorder
Cancer
Blood Disorders
Metabolic Disorders
Immune Disorders
Cancer
- Acute Biphenotypic Leukemia
- Acute Lymphocytic Leukemia (ALL)
- Acute Myelogenous Leukemia (AML)
- Acute Undifferentiated Leukemia
- Adult T Cell Leukemia/Lymphoma
- Chronic Active Epstein Barr
- Chronic Lymphocytic Leukemia (CLL)
- Chronic Myelogenous Leukemia (CML)
- Chronic Myelomonocytic Leukemia (CMML)
- Ewing Sarcoma
- Hodgkin’s Lymphoma
- Juvenile Chronic Myelogenous Leukemia (JCML)
- Juvenile Myelomonocytic Leukemia (JMML)
- Myeloid/Natural Killer (NK) Cell
- PrecursorAcute Leukemia
- Non-Hodgkin’s Lymphoma
- Prolymphocytic Leukemia
- Plasma Cell Leukemia
- Leukocyte Adhesion Deficiency
- Multiple Myeloma
- Neuroblastoma
- Rhabdomyosarcoma
- Thymoma (Thymic Carcinoma)
- Waldenstrom’s Macroglobulinemia
- Wilms Tumor
Blood Disorders
- Acute Myelofibrosis
- Agnogenic Myeloid Metaplasia (Myelofibrosis)
- Amyloidosis
- Aplastic Anemia (Severe)
- Beta Thalassemia Major
- Blackfan-Diamond Anemia
- Congenital Amegakaryocytic Thrombocytopenia (CAT)
- Congenital Cytopenia
- Congenital Dyserythropoietic Anemia
- Dyskeratosis Congenita
- Essential Thrombocythemia
- Fanconi Anemia
- Glanzmann’s Thrombasthenia
- Myelodysplastic Syndrome
- Paroxysmal Nocturnal Hemoglobinuria (PNH)
- Polycythemia Vera
- Pure Red Cell Aplasia
- Refractory Anemia with Excess Blasts (RAEB)
- Refractory Anemia with Excess Blasts in Transition (RAEB-T)
- Refractory Anemia with Ringed Sideroblasts (RARS)
- Shwachman-Diamond Syndrome
- Sickle Cell Disease
Metabolic Disorders
- Congenital Erythropoietic Porphyria (Gunther Disease)
- Gaucher Disease
- Hunter Syndrome (MPS-II)
- Hurler Syndrome (MPS-IH)
- Krabbe Disease
- Lesch-Nyhan Syndrome
- Mannosidosis
- Maroteaux-Lamy Syndrome (MPS-VI)
- Metachromatic Leukodystrophy
- Mucolipidosis II (I-cell Disease)
- Neuronal Ceroid Lipofuscinosis (Batten Disease)
- Niemann-Pick Disease
- Sandhoff Disease
- Sanfilippo Syndrome (MPS-III)
- Scheie Syndrome (MPS-IS)
- Sly Syndrome (MPS-VII)
- Tay Sachs
- Wolman Disease
- X-Linked Adrenoleukodystrophy
Immune Disorders
- Adenosine Deaminase Deficiency (SCID)
- Bare Lymphocyte Syndrome (SCID)
- Chediak-Higashi Syndrome (SCID)
- Chronic Granulomatous Disease
- Congenital Neutropenia
- DiGeorge Syndrome
- Evans Syndrome
- Fucosidosis
- Hemophagocytic Lymphohistiocytosis (HLH)
- Hemophagocytosis Langerhans’ Cell
Histiocytosis (Histiocytosis X) - IKK Gamma Deficiency (NEMO Deficiency)
- Immune Dysregulation, Polyendocrinopathy,
Enteropathy, X-linked (IPEX) Syndrome - Kostmann Syndrome (SCID)
- Myelokathexis
- Omenn Syndrome (SCID)
- Phosphorylase Deficiency (SCID)
- Purine Nucleoside (SCID)
- Reticular Dysgenesis (SCID)
- Severe Combined Immunodeficiency Diseases (SCID)
- Thymic Dysplasia
- Wiskott-Aldrich Syndrome
- X-linked Agammaglobulinemia
- X-Linked Hyper IgM Syndrome
- X-Linked Lymphoproliferative Disorder