Diseases Treated

Acute Leukemias

Acute Lymphoblastic Leumia (ALL)
Acute Myelogenous Leukemia (AML)
Acute Biphenotypic Leukemia
Acute Undifferentiated Leukemia
Acute Lymphoblastic Leukemia (ALL)
Acute Myelogenous Leukemia (AML)
Acute Biphenotypic Leukemia
Acute Undifferentiated Leukemia

Chronic Leukemias

Chronic Myelogenous Leukemia(CML)
Chronic Lymphocytic Leukemia(CLL)
Juvenile Chronic Myelogenous Leukemia (JCML)
Juvenile Myelomonocytic Leukemia (JMML)
Chronic Myelogenous Leukemia (CML)
Chronic Lymphocytic Leukemia (CLL)
Juvenile Chronic Myelogenous Leukemia (JCML)
Juvenile Myelomonocytic Leukemia (JMML)

Inherited Metabolic Disorders (non-mallgnant metabolic)

Mucopolysaccaridoses (MPS)
Hurler’s Syndrome (MPS-IH)
Schele Syndrome (MPS-IS)
Maroteaux-Lamy Syndrome (MPS-VI)
Sly Syndrome, Beta-Glucuronidase Deficiency (MPS-VII)
Adrenoleukodystrophy
Mucolipidosis II (I-cell Disease)
Krabbe Disease
Niemann-Pick Disease
Wolman Disease
Metachromatic Leukudystroph
Mucopolysaccaridoses (MPS)
Hurler’s Syndrome (MPS-IH)
Schele Syndrome (MPS-IS)
Maroteaux-Lamy Syndrome (MPS-VI)
Sly Syndrome, Beta-Glucuronidase Deficiency (MPS-VII)
Adrenoleukodystrophy
Mucolipidosis II (I-cell Disease)
Krabbe Disease
Niemann-Pick Disease
Wolman Disease
Metachromatic Leukudystrophy

Inherited Erythrophagocytic Abnormallties

Beta Thalassemia Major
Sickle Cell Disease
Beta Thalassemia Major
Sickle Cell Disease

Histiocytic Disorders

Familial Erythrophagocytic Lymphohistuictosis
Histiocytosis-X
Hemophagocytosis
Familial Erythrophagocytic Lymphohistuictosis
Histiocytosis-X
Hemophagocytosis

InheritedImmuneSystemDisorders(nonmalignantimmunedeficiency,primaryimmunedeficiency)

Ataxia-Telangiectasia
Kostmann Syndrome
Leukocyte Adhesion Deficiency
DiGeroge Syndrome
Bare Lymphocyte Syndrome
Omenn’s Syndrome
Servere Combined Immunodeficiency (SCID)
SCID with Adenosine Deaminase Deficiency
Absence of T & B Cells SCID
Absence of T Cells, Normal B Cell SCID
Common Variable Immunodeficiency
Wishkott-Aldrich Syndrome
X-Linked Lymphoproliferative Disorder

Inherited Platelet Abnormallties (acquired marrow failure)

Amegakaryocytosis/Congenital Thrombocytopenia

Lymphoproliferative Disorders

Non-Hodgkin’s Lymphoma
Hodgkin’s Disease

Myelodysplastic Syndromes (MDS)

Refractory Cytopenia with Unillineage Dysplasia
Rafractory Anemia with Ring Siderobiasts
Refractory Anemia with Multilineage Dysplasia
Refractory Anemia with Excess Blasts
5 q- Syndrome
Refractory Cytopenia of Childhood
Myelodysplasia Unclassifiable

Myeloproliferative Disorders

Acute Myelofibrosis
Agenogenic Myeloid Metaplasia
Polycythemia Vera
Essential Thrombocythemia

Myeloproliferative/Myerlodysplastic Overlay Sndromes

Refractory anemia with Ringed Sideroblastic Therombocytosis
Chronic Myelomonocytic Leukemia

Other Inherited Disorders

Cartilage-Hair Hypoplasia
Glanzmann Thrombasthenia
Osteopetrosis

Phagocyte Disorders (Non-mallgnant Immune deficiency)

Chediak-Higashi Syndrome
Chronic Granulomatous Disease
Neutrophil Action Deficiency
Reticullar Dysgensis

Stem Call Disorders (Acquired marrow failure)

Aplastic Anemia (Severe)
Fanconi Anemia
Paroxysmal Nocturnal Hemoglobinuria (PNH)
Pure Red Cell Aplasia

Plasma Cell Disorders

Multiple Myeloma
Waldenstrome’s Macroglobulinemia

Reprinted by permission from Be the Match Foundation ® which supports the National Marrow Donor Program ® a leader in the field of marrow and cord blood transfusion.