List of conditions treated with hematopoietic stem cell transplantation

Hematopoietic stem cell transplantation may be used to treat a number of conditions both congenital and acquired.

Acquired

 * Malignancies
 * Hematological
 * Leukemias
 * Acute lymphoblastic leukemia (ALL)
 * Acute myeloid leukemia (AML)
 * Chronic lymphocytic leukemia (CLL)
 * Chronic myelogenous leukemia (CML), accelerated phase or blast crisis
 * Lymphomas
 * Hodgkin's disease
 * Non-Hodgkin's lymphoma
 * Myelomas
 * Multiple myeloma (Kahler's disease)
 * Solid tumor cancers
 * Neuroblastoma
 * Desmoplastic small round cell tumor
 * Ewing's sarcoma
 * Choriocarcinoma
 * Hematologic disease
 * Phagocyte disorders
 * Myelodysplasia
 * Anemias
 * Paroxysmal nocturnal hemoglobinuria (PNH; severe aplasia)
 * Aplastic anemia
 * Acquired pure red cell aplasia
 * Myeloproliferative disorders
 * Polycythemia vera
 * Essential thrombocytosis
 * Myelofibrosis
 * Metabolic disorders
 * Amyloidoses
 * Amyloid light chain (AL) amyloidosis
 * Environmentally-induced diseases
 * Radiation poisoning
 * Viral diseases
 * HTLV
 * HIV
 * Autoimmune diseases
 * Multiple sclerosis

Congenital

 * Lysosomal storage disorders
 * Lipidoses (disorders of lipid storage)
 * Neuronal ceroid lipofuscinoses
 * Infantile neuronal ceroid lipofuscinosis (INCL, Santavuori disease,)
 * Jansky–Bielschowsky disease (late infantile neuronal ceroid lipofuscinosis)
 * Sphingolipidoses
 * Niemann–Pick disease
 * Gaucher disease
 * Leukodystrophies
 * Adrenoleukodystrophy
 * Metachromatic leukodystrophy
 * Krabbe disease (globoid cell leukodystrophy)
 * Mucopolysaccharidoses
 * Hurler syndrome (MPS I H, α-L-iduronidase deficiency)
 * Scheie syndrome (MPS I S)
 * Hurler–Scheie syndrome (MPS I H-S)
 * Hunter syndrome (MPS II, iduronidase sulfate deficiency)
 * Sanfilippo syndrome (MPS III)
 * Morquio syndrome (MPS IV)
 * Maroteaux–Lamy syndrome (MPS VI)
 * Sly syndrome (MPS VII)
 * Glycoproteinoses
 * Mucolipidosis II (I-cell disease)
 * Fucosidosis
 * Aspartylglucosaminuria
 * Alpha-mannosidosis
 * Other
 * Wolman disease (acid lipase deficiency)
 * Immunodeficiencies
 * T-cell deficiencies
 * Ataxia-telangiectasia
 * DiGeorge syndrome
 * Combined T- and B-cell deficiencies
 * Severe combined immunodeficiency (SCID), all types
 * Well-defined syndromes
 * Wiskott–Aldrich syndrome
 * Phagocyte disorders
 * Kostmann syndrome
 * Shwachman–Diamond syndrome
 * Immune dysregulation diseases
 * Griscelli syndrome, type II
 * Innate immune deficiencies
 * NF-Kappa-B Essential Modulator (NEMO) deficiency (Inhibitor of Kappa Light Polypeptide Gene Enhancer in B Cells Gamma Kinase deficiency)
 * Hematologic diseases
 * Hemoglobinopathies
 * Sickle cell disease
 * β thalassemia major (Cooley's anemia)
 * Anemias
 * Aplastic anemia
 * Diamond–Blackfan anemia
 * Fanconi anemia
 * Cytopenias
 * Amegakaryocytic thrombocytopenia
 * Hemophagocytic syndromes
 * Hemophagocytic lymphohistiocytosis (HLH)