U.S. Transplant Centers
We partner with more than 150 transplant centers across the United States to facilitate blood stem cell transplants, support patients and conduct research.
Search for a U.S. transplant center
If you are a patient or family member looking for a transplant center, our transplant center search tool can help. You can search by state or diagnosis or look at the listing of all U.S. transplant centers.
You’ll get an overview of the center and learn more about the number of transplants each center has facilitated, the type of transplant performed, outcomes data and other information that can help you find a center that best meets your needs.
If you have questions or aren't finding a center near you, contact us.
Call: +1 (888) 999-6743 or (763) 406-3410Monday through Friday, 8 a.m.-5 p.m. Central Time
EMAIL: patientinfo@nmdp.org
Diagnosis(optional)
Acute lymphoblastic leukemia (ALL)
Acute myeloid leukemia (AML)
Acquired pure red cell aplasia
Amegakaryocytosis (not congenital)
Aplastic anemia
Other stem cell disorder
Severe aplastic anemia
Autoimmune Disease
Crohn’s disease
Evans syndrome
Hemolytic anemia
Juvenile idiopathic arthritis: oligoarticular
Multiple sclerosis
Other autoimmune disease
Systemic sclerosis (scleroderma)
Atypical chronic myeloid leukemia
Chronic myeloid leukemia (CML)
Juvenile Chronic Myelogenous Leukemia (JCML)
Myelodysplastic Syndrome (MDS)
Unknown Myelodysplastic Disorder (UMDS)
Beta thalassemia major
Hemoglobinopathies
Other hemoglobinopathy
Sickle cell anemia
Familial Hemophagocytic Lymphohistiocytosis
Hemophagocytic lymphohistiocytosis (HLH)
Hemophagocytosis
Histiocytic disease
Langerhans cell histiocytosis
Malignant histiocytosis
Other histiocytic disease
Hodgkin lymphoma
Diamond-blackfan anemia
Paroxysmal Nocturnal Hemoglobinuria (PNH)
Fanconi anemia
Inherited bone marrow failure
Kostmann syndrome (congenital neutropenia)
Other inherited bone marrow failure syndrome
Other inherited erythrocyte abnormalities
Shwachmann-diamond syndrome
Adrenoleukodystrophy (ALD)
Aspartyl Glucosaminidase (ASPGL)
Beta-glucuronidase deficiency (VII)
Fucosidosis (FUCOSI)
Gaucher Disease (GAUCHR)
Glucose Storage Disease (GLUCST)
Hereditary diffuse leukoencephalopathy with spheroids (HDLS)
Hunter syndrome
Hurler syndrome (mps-ih or mps i)
I-Cell Disease (ICELL)
Inherited disorders of metabolism
Krabbe disease
Lesch-Nyhan Syndrome (LNS)
Lysosomal Storage Disease (LYSOST)
Mannosidosis
Maroteaux-lamy
Metachromatic leukodystrophy (MLD)
Morquio Syndrome (MPS-IV) (MORQUO)
Morquio Syndrome Type A (MPS IVA) (MORQUA)
Morquio Syndrome Type B (MPS IVB) (MORQUB)
Mucopolysaccharidosis (MPS-V) (MPS)
Mucopolysaccharidosis, not otherwise specified
Neuronal ceriod - lipofuscinosis (Batten disease)
Neuronal Ceroid Lipofuscinosis 2 (NCL2)
Niemann-Pick Disease (N-P)
Osteopetrosis
Other metabolic disorders
Other Mucopolysaccharidosis (OIMDP)
Sanfilippo A (MPS IIIA) (SANFIA)
Sanfilippo B (MPS IIIB) (SANFIB)
Sanfilippo C (MPS IIIC) (SANFIC)
Sanfilippo D (MPS IIID) (SANFID)
Sanfilippo (III)
Scheie Syndrome (MPS-IS) (SCHEIE)
Wolman disease
Ataxia-Telangiectasia (AT)
Bare lymphocyte syndrome
Cartilage hair hypoplasia
CD4 ligand deficiency
Chediak-higashi syndrome
Chronic granulomatous disease
Combined Immunodeficiency (CID)
Common variable immunodeficiency
DiGeorge anomaly
Immune Deficiency + Neutropenia (IMDNP)
Immune deficiency, not otherwise specified
Inherited immune system disorders
Kostmann's Agranulocytosis (KOSTMN)
Leukocyte adhesion deficiency
Neutrophil Actin Deficiency (NEUTAD)
Omenn syndrome
Other Combined Immunodeficiency (OCID)
Other Immune System (OIIS)
Other Severe Combined Immunodeficiency (OSCID)
Reticular dysgenesis
SCID with Absence of T & B Cells (TBSCID)
SCID with Absence of T Cells, Normal B Cells (TSCID)
SCID with Adenosine Deaminase Deficiency (SCIDAD)
Severe combined immunodeficiency (SCID)
Wiskott-Aldrich syndrome (WAS)
X-linked lymphoproliferative syndrome
Congenital amegakaryocytosis/congenital thrombocytopenia
Glanzmann thrombasthenia
Inherited platelet abnormalities
Other inherited platelet abnormality
Multiple myeloma
Multiple myeloma / Plasma cell disease
Other plasma cell disorders
Plasma Cell Leukemia (PCL)
Unknown Plasma Cell Disorder (UPCD)
Chronic myelomonocytic leukemia
Juvenile chronic myelomonocytic leukemia
Acquired Idiopathic Sideroblastic Anemia (AISA)
Myelodysplastic diseases (MDS)
Other Myelodysplastic Disorder (OMDS)
Other Myelofibrosis/Myelosclerosis (OMF)
Refractory Anemia (RA)
Refractory Anemia w/ Excess Blasts (RAEB)
Refractory Anemia w/ Excess Blasts in Transformation (RAEBIT)
Acute Mast Cell Leukemia (AMCL)
Chronic eosinophilic leukemia (hypereosinophilic syndrome)
Chronic neutrophilic leukemia
Essential thrombocythemia
Myeloproliferative diseases (MPS)
Other myeloproliferative diseases
Polycythemia vera
Primary myelofibrosis
Non-Hodgkin lymphoma
Waldenstrom Macroglobulinemia (WMG)
Other Disease
Other Non-Malignant Disease, Specify (OND)
Chronic lymphocytic leukemia (CLL)
Other Leukemia
Acute Bilineage Leukemia (ABL)
Acute Undifferentiated Leukemia (AUL)
Hairy Cell Leukemia (HCL)
Other leukemia - not otherwise specified
Prolymphocytic Leukemia (PHILLY)
Bone sarcoma
Breast Cancer (BRCA)
Central nervous system tumor
Other Malignancy, Specify (OMS)
Small Cell Lung Cancer (SCLUNG)
Ewing family of tumors bone (includes PNET)
Ewing family of tumors extra-osseous (includes PNET)
Germ cell tumors
Head and neck cancer
Mediastinal neoplasm
Medulloblastoma
Neuroblastoma
Other solid tumors
Ovary
Renal cell carcinoma
Retinoblastoma
Rhabdomyosarcoma
Soft tissue sarcoma
Solid tumors
Testicular
Wilm tumor
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