Center Number
State of transplant center
Age group: 0-5 years old
Age group: 11-17 years old
Age group: 18-34 years old
Age group: 35-49 years old
Age group: 50-64 years old
Age group: 65-70 years old
Age group: 6-10 years old
Age group: 71-75 years old
Age group: greater than 76 years old
Bone Marrow
Cord Blood
Peripheral Blood
HSCT
Disease Category: Autoimmune Disease (AI)
Disease category: Acute lymphoblastic leukemia (ALL)
Disease category: Acute myelogenous leukemia (AML)
Disease_category: Aplastic Anemia (AA)
Disease category: Chronic myelogenous leukemia (CML)
Disease category: Histiocytic disease (HIS)
Disease category: Hodgkin lymphoma (HL)
Disease category: Hemoglobinopathies
Disease category: Inherited bone marrow failure syndromes (IBMFS)
Disease category: Inherited abnormalities of erythrocyte differentiation or function (IEA)
Disease category: Disorders of the immune system (IIS)
Disease category: Inherited disorders of metabolism (IMD)
Disease category: Inherited platelet abnormalities (IPA)
Disease category: Myelodysplastic diseases (MDS)
Disease category: Myelodysplastic/Myeloproliferative diseases (MDS/MPN)
Disease category: Multiple myeloma (MM)
Disease category: Myeloproliferative diseases (MPN)
Disease category: Non Hodgkin lymphoma (NHL)
Disease category: Acute leukemia, other (OAL)
Disease category: Other disease (OND)
Disease category: Leukemia, other (OTH_LEUK)
Disease category: Plasma cell disease (PCD)
Disease category: Paroxysmal nocturnal hemoglobinuria (PNH)
Disease category: Solid tumors (STU)
1st Remission
2nd or subsequent remission
Data unavailanble
In remission
Not applicable
Not in remission
Autologous
HLA-matching sibling
Related donor
Unrelated
Data unavailable
Hispanic or Latino
Not Hispanic or Latino
Specific disease on form: Mixed phenotype acute leukemia, T/myeloid, NOS
Specific disease on form: Acquired aplastic anemia, not otherwise specified
Specific disease on form: Acquired amegakaryocytosis (not congenital)
Specific disease on form: Acquired pure red cell aplasia (not congenital)
Specific disease on form: Acquired AA secondary to toxin/other drug
Specific disease on form: Other acquired cytopenic syndrome
Specific disease on form: Acquired AA secondary to hepatitis
Specific disease on form: Antiphospholipid syndrome
Specific disease on form: Churg-Strauss
Specific disease on form: Crohn's disease
Specific disease on form: Evan syndrome
Specific disease on form: Hemolytic anemia
Specific disease on form: Idiopathic thrombocytopenic purpura (ITP)
Specific disease on form: Juvenile idiopathc arthritis (JIA): systemic (Stills disease)
Specific disease on form: JIA: polyarticular
Specific disease on form: Multiple sclerosis
Specific disease on form: Other autoimmune bowel disorder
Specific disease on form: Other autoimmune cytopenia
Specific disease on form: Other autoimmune neurological disorder
Specific disease on form: Other connective tissue disease
Specific disease on form: Other vasculitis
Specific disease on form: Systemic lupus erythematosis (SLE)
Specific disease on form: Systemic sclerosis (scleroderma)
Specific disease on form: Myasthenia gravis
Specific disease on form: Other autoimmune disease
Specific disease on form: BCR-ABL1-like
Specific disease on form: B-cell ALL, not otherwise specified {L1/L2}
Specific disease on form: Hyperdiploidy (51-65 chromosomes)
Specific disease on form: Hypodiploidy (<46 chromosomes)
Specific disease on form: Natural killer (NK)- cell lymphoblastic leukemia / lymphoma (provisional entity)
Specific disease on form: ALL, not otherwise specified
Specific disease on form: Precursor T-cell ALL
Specific disease on form: Precursor T-lymphoblastic lymphoma / leukemia
Specific disease on form: B-lymphoblastic leukemia / lymphoma, with iAMP21 (provisional entity)
Specific disease on form: t(v;11q23); MLL rearranged
Specific disease on form: t(12;21)(p12;q22) TEL-AML1
Specific disease on form: t(1;19)(q23;p13.3) E2A/PBX1
Specific disease on form: t(5;14) (q31;q32); IL3-IGH
Specific disease on form: t(9;22)(q34;q11); BCR/ABL1
Specific disease on form: AML with 11q23 (MLL) abnormalities
Specific disease on form: AML or ANLL, not otherwise specified
Specific disease on form: APL with t(15;17)(q22;q12); PML-RARA
Specific disease on form: Acute Erythroid Leukemia (erythroid / myeloid and pure erythroleukemia) (M6)
Specific disease on form: Acute megakaryoblastic leukemia (M7)
Specific disease on form: Acute monoblastic / acute monocytic leukemia (M5)
Specific disease on form: Acute myelomonocytic leukemia (M4)
Specific disease on form: Acute panmyelosis with myelofibrosis
Specific disease on form: AML with BCR-ABL1 (provisional entity)
Specific disease on form: AML with biallelic mutations of CEBPA
Specific disease on form: AML with inv(16); (p13;1q22) or t(16;16) (p13.1; q22); CBFB/MYH11
Specific disease on form: AML with t(6;9) (p23;q24); DEK-NUP214
Specific disease on form: AML with t(9;11) (p22;q23); MLLT 3-MLL
Specific disease on form: AML with maturation (M2)
Specific disease on form: AML (megakaryoblastic) with t(1;22) (p13;q13); RBM15-MKL1
Specific disease on form: AML, minimally differentiated (M0)
Specific disease on form: AML with myelodysplasia related changes
Specific disease on form: Myeloid sarcoma
Specific disease on form: AML with mutated NPM1
Specific disease on form: AML without maturation (M1)
Specific disease on form: AML with inv(3) (q21;q26.2) or t(3;3) (q21;q26.2); RPN1-EVI1 (7)
Specific disease on form: AML with mutated RUNX1 (provisional entity)
Specific disease on form: AML with t(8;21); (q22; q22); RUNX1/RUNX1T1
Specific disease on form: Therapy related AML (t-AML)
Specific disease on form: Blastic plasmacytoid dendritic cell neoplasm
Specific disease on form: Myeloid leukemia associated with Down syndrome
Specific disease on form: Other hemoglobinopathy
Specific disease on form: Sickle cell disease
Specific disease on form: Transfusion dependent thalassemia
Specific disease on form: Familial erythrohemophagocytic lymphohistiocytosis (FELH)
Specific disease on form: Hemophagocytosis (reactive or viral associated)
Specific disease on form: Langerhans cell histiocytosis (histiocytosis-X)
Specific disease on form: Malignant histiocytosis
Specific disease on form: Histiocytic disorder, not otherwise specified
Specific disease on form: Other histiocytic disorder
Specific disease on form: Lymphocyte depleted
Specific disease on form: Lymphocyte rich
Specific disease on form: Mixed cellularity
Specific disease on form: Hodgkin lymphoma, not otherwise specified
Specific disease on form: Nodular lymphocyte predominant Hodgkin lymphoma
Specific disease on form: Nodular sclerosis
Diamond-Specific disease on form: Blackfan anemia (pure red cell aplasia)
Specific disease on form: Dyskeratosis congenita
Specific disease on form: Fanconi anemia
Specific disease on form: Kostmann agranulocytosis (congenital neutropenia)
Specific disease on form: Shwachman-Diamond
Specific disease on form: Other constitutional anemia
Specific disease on form: Bare lymphocyte syndrome
Specific disease on form: CD40 ligand deficiency
Specific disease on form: Cartilage-hair hypoplasia
Specific disease on form: Chediak-Higashi syndrome
Specific disease on form: Chronic granulomatous disease
Specific disease on form: Common variable immunodeficiency
Specific disease on form: Griscelli syndrome type
Specific disease on form: HIV infection
Specific disease on form: Leukocyte adhesion deficiencies, including GP180, CD-18, LFA and WBC adhesion deficiencies
Specific disease on form: Omenn syndrome
Specific disease on form: Other immunodeficiencies
Specific disease on form: Other SCID
Specific disease on form: Reticular dysgenesis
Specific disease on form: Adenosine deaminase (ADA) deficiency / severe combined immunodeficiency (SCID)
Specific disease on form: SCID, not otherwise specified
Specific disease on form: Absence of T and B cells SCID
Specific disease on form: Absence of T, normal B cell SCID
Specific disease on form: Wiskott-Aldrich syndrome
Specific disease on form: X-linked lymphoproliferative syndrome
Specific disease on form: Immune deficiency, not otherwise specified
Specific disease on form: Adrenoleukodystrophy (ALD)
Specific disease on form: Fucosidosis
Specific disease on form: Gaucher disease
Specific disease on form: Hunter syndrome (II)
Specific disease on form: Hurler syndrome (IH)
Specific disease on form: Krabbe disease (Globoid leukodystrophy)
Specific disease on form: Metachromatic leukodystrophy (MLD)
Specific disease on form: Mannosidosis
Specific disease on form: Morquio (IV)
Specific disease on form: Mucopolysaccharidosis (V)
Specific disease on form: Inherited metabolic disorder, not otherwise specified
Specific disease on form: Neimann - Pick disease
Specific disease on form: Neuronalceriod - lipofuscinosis (Batten disease)
Specific disease on form: Osteopetrosis (malignant infantile osteopetrosis)
Specific disease on form: Other inherited metabolic disorder
Specific disease on form: Sanfilippo (III)
Specific disease on form: Congenital amegakaryocytosis / congenital thrombocytopenia
Specific disease on form: Glanzmann thrombasthenia
Specific disease on form: Other inherited platelet abnormality
Specific disease on form: 5q minus syndrome
Specific disease on form: Refractory cytopenia of childhood
Specific disease on form: Chronic myelomonocytic leukemia (CMMoL)
Specific disease on form: Juvenile myelomonocytic leukemia (JMML, JCML, JCMML) (no evidence of Ph1 or BCR/ABL)
Specific disease on form: MDS / MPN with ring sideroblasts and thrombocytosis (MDS / MPN-RS-T)
Specific disease on form: Myelodysplastic / myeloproliferative neoplasm, unclassifiable
Specific disease on form: Atypical chronic myeloid leukemia (aCML), BCR-ABL1-
Specific disease on form: Atypical chronic myeloid leukemia, Ph-/BCR/ABL-
Specific disease on form: Atypical chronic myeloid leukemia, Ph-/BCR unknown
Specific disease on form: Atypical chronic myeloid leukemia, Ph unknown/BCR-
Specific disease on form: Mastocytosis
Specific disease on form: RARS
Specific disease on form: Refractory cytopenia with unilineage dysplasia (RCUD) (includes refractory anemia (RA))
Specific disease on form: MDS-RS with multilineage dysplasia
Specific disease on form: MDS unclassifiable, not otherwise specified
Specific disease on form: Myelodysplastic syndrome with multilineage dysplasia
Specific disease on form: Myeloid / lymphoid neoplasms with FGFR1 rearrangement
Specific disease on form: Myeloid / lymphoid neoplasms with PCM1-JAK2
Specific disease on form: Myeloid / lymphoid neoplasms with PDGFRB rearrangement
Specific disease on form: Myelodysplastic syndrome with single lineage dysplasia
Specific disease on form: MDS with excess blasts-1
Specific disease on form: MDS with excess blasts-2
Specific disease on form: Multiple myeloma-IgM (not Waldenstrom macroglobulinemia)
Specific disease on form: Multiple myeloma-light chain only
Specific disease on form: Multiple myeloma, not otherwise specified
Specific disease on form: Multiple myeloma-non-secretory
Specific disease on form: Smoldering myeloma
Specific disease on form: Multiple myeloma-IgA
Specific disease on form: Multiple myeloma-IgD
Specific disease on form: Multiple myeloma-IgE
Specific disease on form: Multiple myeloma-IgG
Specific disease on form: Multiple myeloma-Multiple Chain
Specific disease on form: Chronic eosinophilic leukemia (hypereosinophilic syndrome)
Specific disease on form: Chronic neutrophilic leukemia
Specific disease on form: Essential thrombocythemia
Specific disease on form: Polycythemia vera
Specific disease on form: Post-essential thrombocythemic myelofibrosis
Specific disease on form: Post-polycythemic myelofibrosis
Specific disease on form: Primary myelofibrosis (includes chronic idiopathic myelofibrosis (CIMF), angiogenic myeloid metaplasia (AMM), myelofibrosis/sclerosis with myeloid metaplasia (MMM), idiopathic myelofibrosis)
Specific disease on form: Myeloproliferative neoplasm (MPN), unclassifiable
Specific disease on form: Systemic mastocytosis
Specific disease on form: Anaplastic large-cell lymphoma (ALCL), ALK negative
Specific disease on form: Anaplastic large-cell lymphoma (ALCL), ALK positive
Specific disease on form: Adult T-cell lymphoma/leukemia
Specific disease on form: Aggressive NK-cell leukemia
Specific disease on form: Angioimmunoblastic T-cell lymphoma
Specific disease on form: Burkitt lymphoma
Specific disease on form: Chronic lymphoproliferative disorder of NK cells
Specific disease on form: Classical Hodgkin lymphoma PTLD
Specific disease on form: Primary cutaneous CD30+ T-cell lymphoproliferative disorders
Specific disease on form: Primary cutaneous CD4+ small / medium T-cell lymphoproliferative disorder
Specific disease on form: Primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma
Specific disease on form: Primary cutaneous DLBCL, leg type
Specific disease on form: Primary cutaneous gamma-delta T-cell lymphoma
Specific disease on form: Diffuse, large B-cell lymphoma- Germinal center B-cell type
Specific disease on form: DLBCL associated with chronic inflammation
Specific disease on form: Diffuse, large B-cell lymphoma- Activated B-cell type (non-GCB)
Specific disease on form: Diffuse, Large B-cell Lymphoma (cell of origin unknown)
Specific disease on form: EBV+ DLBCL, NOS
Specific disease on form: EBV+ mucocutaneous ulcer
Specific disease on form: Enteropathy-type T-cell lymphoma
Specific disease on form: Extranodal NK / T-cell lymphoma, nasal type
Specific disease on form: Extranodal marginal zone B-cell lymphoma of mucosal associated lymphoid tissue type
Specific disease on form: Follicular lymphoma grade I
Specific disease on form: Follicular lymphoma grade II
Specific disease on form: Follicular lymphoma grade unknown
Specific disease on form: Follicular, predominantly large cell (Grade IIIA follicle center lymphoma)
Specific disease on form: Follicular, predominantly large cell (Grade IIIB follicle center lymphoma)
Specific disease on form: Follicular, predominantly large cell (Grade IIIA vs IIIB not specified)
Specific disease on form: Follicular T-cell lymphoma
Specific disease on form: HHV8+ DLBCL, NOS
Specific disease on form: Hepatosplenic T-cell lymphoma
Specific disease on form: High-grade B-cell lymphoma, with MYC and BCL2 and/or BCL6 rearrangements
Specific disease on form: High-grade B-cell lymphoma, NOS
Specific disease on form: Intravascular large B-cell lymphoma
Specific disease on form: Large B-cell lymphoma with IRF4 rearrangement
Specific disease on form: ALK+ large B-cell lymphoma
Specific disease on form: T-cell large granular lymphocytic leukemia
Specific disease on form: Lymphomatoid granulomatosis
Specific disease on form: Lymphoplasmacytic lymphoma/ Waldenstrom macroglobulinemia
Specific disease on form: Mantle cell lymphoma
Specific disease on form: Monomorphic epitheliotropic intestinal T-cell lymphoma
Specific disease on form: Monomorphic PTLD (B- and T-/NK-cell types)
Specific disease on form: Mycosis fungoides
Specific disease on form: Nodal marginal zone B-cell lymphoma
Specific disease on form: Nodal peripheral T-cell lymphoma with TFH phenotype
Specific disease on form: Other B-cell lymphoma
Specific disease on form: Other T-cell/NK-cell lymphoma
Specific disease on form: Peripheral T-cell lymphoma (PTCL), NOS
Specific disease on form: Plasmablastic lymphoma
Specific disease on form: Plasmacytic hyperplasia PTLD
Specific disease on form: Primary CNS lymphoma
Specific disease on form: Primary effusion lymphoma
Specific disease on form: Primary mediastinal (thymic) large B-cell lymphoma
Specific disease on form: Sezary syndrome
Specific disease on form: Splenic marginal zone B-cell lymphoma
Specific disease on form: Subcutaneous panniculitis-like T-cell lymphoma
Specific disease on form: Systemic EBV+ T-cell lymphoma of childhood
Specific disease on form: T-cell / histiocytic rich large B-cell lymphoma
Specific disease on form: B-cell lymphoma, unclassifiable, with features intermediate between DLBCL and classical Hodgkin Lymphoma
Specific disease on form: Breast implant-associated anaplastic large-cell lymphoma
Specific disease on form: Primary cutaneous follicle center lymphoma
Specific disease on form: Splenic diffuse red pulp small B-cell lymphoma
Specific disease on form: Polymorphic PTLD
Specific disease on form: Indolent T-cell lymphoproliferative disorder of the GI tract
Specific disease on form: Biphenotypic, bilineage or hybrid leukemia
Specific disease on form: Mixed phenotype acute leukemia with t(v; 11q23.3); KMT2A rearranged
Specific disease on form: Mixed phenotype acute leukemia (MPAL) with t(9;22)(q34.1;q11.2); BCR-ABL1
Specific disease on form: Mixed phenotype acute leukemia, B/myeloid, NOS
Specific disease on form: Other acute leukemia
Specific disease on form: Acute undifferentiated leukemia
Specific disease on form: Other disease
Specific disease on form: Other leukemia
Specific disease on form: Chronic lymphocytic leukemia (CLL), not otherwise specified
Specific disease on form: CLL, B-cell / small lymphocytic lymphoma
Specific disease on form: Prolymphocytic Leukemia (PLL), not otherwise specified
Specific disease on form: PLL, B-cell
Specific disease on form: PLL, T-cell
Specific disease on form: Monoclonal gammopathy of renal significance (MGRS)
Specific disease on form: Other PCD, specify
Specific disease on form: Osteosclerotic myeloma / POEMS syndrome
Specific disease on form: Plasma cell leukemia
Specific disease on form: Primary amyloidosis
Specific disease on form: Solitary plasmacytoma
Specific disease on form: Paroxysmal nocturnal hemoglobinuria
Specific disease on form: Bone sarcoma, excluding Ewing family tumors
Specific disease on form: Central nervous system tumor, including CNS PNET
Specific disease on form: Ewing family tumors of bone (includes PNET)
Specific disease on form: Ewing family tumors, extra-osseous (includes PNET)
Specific disease on form: External genitalia
Specific disease on form: Germ cell tumor, extragonadal
Specific disease on form: Head / neck
Specific disease on form: Mediastinal neoplasm
Specific disease on form: Medulloblastoma
Specific disease on form: Melanoma
Specific disease on form: Solid tumor, not otherwise specified
Specific disease on form: Neuroblastoma
Specific disease on form: Neurogenic sarcoma
Specific disease on form: Other solid tumor
Specific disease on form: Ovarian (epitheleal)
Specific disease on form: Pancreatic
Specific disease on form: Prostate
Specific disease on form: Retinoblastoma
Specific disease on form: Rhabdomyosarcoma
Specific disease on form: Soft tissue sarcoma (excluding Ewing family tumors)
Specific disease on form: Testicular
Specific disease on form: Wilm tumor
Specific disease on form: Synovial sarcoma
Specific disease on form: Unknown
American Indian or Alaska Native
Asian
Black or African American
Native Hawaiian or other Pacific Islander
Multiple race
White
Specific disease:AA - Acquired pure red cell aplasia
Specific disease:AA - Amegakaryocytosis (not congenital)
Specific disease:AA - Aplastic anemia
Specific disease:AI - Antiphospholipid syndrome
Specific disease:AI - Churg-Strauss
Specific disease:AI - Crohns disease
Specific disease:AI - Evan syndrome
Specific disease:AI - Hemolytic anemia
Specific disease:AI - Idiopathic thrombocytopenic purpura (ITP)
Specific disease:AI - Multiple sclerosis
Specific disease:AI - Other autoimmune bowel disease
Specific disease:AI - Other autoimmune cytopenia (low blood counts)
Specific disease:AI - Other vasculitis
Specific disease:AI - Juvenile idiopathic arthritis: polyarticular
Specific disease:AI - Juvenile idiopathic arthritis systemic (Stills disease)
Specific disease:AI - Myasthenia gravis
Specific disease:AI - Other autoimmune neurologic disease
Specific disease:AI - Other connective tissue disease
Specific disease:AI - Other autoimmune disease
Specific disease:AI - Scleroderma/systemic sclerosis
Specific disease:AI - Systemic lupus erythematosis
Specific disease:ALL - t(v;11q23); MLL rearranged
Specific disease:ALL - BCR-ABL1-like
Specific disease:ALL - Natural killer (NK)- cell lymphoblastic leukemia / lymphoma (provisional entity)
Specific disease:ALL - Not otherwise specified
Specific disease:ALL - Precursor T-cell ALL
Specific disease:ALL - B-lymphoblastic leukemia / lymphoma, with iAMP21 (provisional entity)
Specific disease:ALL - Hyperdiploidy (51-65 chromosomes)
Specific disease:ALL - Hypodiploidy (<46 chromosomes)
Specific disease:ALL - Precursor T-lymphoblastic lymphoma / leukemia
Specific disease:ALL - t(12;21)
Specific disease:ALL - t(1;19)
Specific disease:ALL - t(5;14)
Specific disease:ALL - t(9;22)
Specific disease:AML - with 11q23 (MLL) abnormalities (i.e., t(4;11), t(6;11), t(9;11), t(11;19))
Specific disease:AML - APL with t(15;17) and variant (M3)
Specific disease:AML - AML with BCR-ABL1 (provisional entity)
Specific disease:AML - Myeloid sarcoma
Specific disease:AML - Not otherwise specified
Specific disease:AML - With mutated NPM1
Specific disease:AML - AML with mutated RUNX1 (provisional entity)
Specific disease:AML - Acute erythroid leukemia (erythroid / myeloid and pure erythroleukemia) (M6)
Specific disease:AML - Acute megakaryoblastic leukemia (M7)
Specific disease:AML - Acute monoblastic / acute monocytic leukemia (M5)
Specific disease:AML - Acute myelomonocytic leukemia (M4)
Specific disease:AML - Acute panmyelosis with myelofibrosis
Specific disease:AML - with biallelic mutations of CEBPA
Specific disease:AML - Myeloid leukemia associated with Down syndrome
Specific disease:AML - with inv(16); or t(16;16)
Specific disease:AML - with inv(3) or t(3;3)
Specific disease:AML - with maturation (M2)
Specific disease:AML - Megakaryoblastic with t(1;22)
Specific disease:AML - Minimally differentiated (M0)
Specific disease:AML - with myelodysplasia - related changes
Specific disease:AML - without maturation (M1)
Specific disease:AML - with t(6;9)
Specific disease:AML - with t(8;21)
Specific disease:AML - with t(9;11)
Specific disease:AML - Therapy related AML (t-AML)
Specific disease:CML - Chronic Myelogenous Leukemia
Specific disease:HEMOGLOB - Sickle cell anemia
Specific disease:HEMOGLOB - Other hemoglobinopathy
Specific disease:HEMOGLOB - Transfusion dependent thalassemia
Specific disease:HIS - Hemophagocytosis
Specific disease:HIS - Not otherwise specified
Specific disease:HIS - Other histiocytic disease
Specific disease:HIS - Hemophagocytic lymphohistiocytosis
Specific disease:HIS - Langerhans cell histiocytosis
Specific disease:HIS - Malignant histiocytosis
Specific disease:HL - Classical Hodgkin lymphoma PTLD
Specific disease:HL - Lymphocyte depleted
Specific disease:HL - Lymphocyte rich
Specific disease:HL - Mixed cellularity
Specific disease:HL - Not otherwise specified
Specific disease:HL - Nodular sclerosis
Specific disease:HL - Nodular lymphocyte predominant
Specific disease:IBMFS - Diamond-blackfan anemia
Specific disease:IBMFS - Dyskeratosis congenita
Specific disease:IBMFS - Fanconi anemia
Specific disease:IBMFS - Kostmann syndrome (congenital neutropenia)
Specific disease:IBMFS - Shwachmann-diamond syndrome
Specific disease:IEA - Other constitutional anemia
Specific disease:IIS - Bare lymphocyte syndrome
Specific disease:IIS - CD40 ligand deficiency
Specific disease:IIS - Cartilage hair hypoplasia
Specific disease:IIS - Chediak-higashi syndrome
Specific disease:IIS - Chronic granulomatous disease
Specific disease:IIS - Common variable immunodeficiency
Specific disease:IIS - Griscelli syndrome type
Specific disease:IIS - HIV infection
Specific disease:IIS - Immune deficiency
Specific disease:IIS - Leukocyte adhesion deficiency
Specific disease:IIS - Not otherwise specified
Specific disease:IIS - Omenn syndrome
Specific disease:IIS - Reticular dysgenesis
Specific disease:IIS - Severe combined immunodeficiency (SCID)
Specific disease:IIS - Wiskott-Aldrich syndrome (WAS)
Specific disease:IIS - X-linked lymphoproliferative syndrome
Specific disease:IMD - Adrenoleukodystrophy (ALD)
Specific disease:IMD - Fucosidosis
Specific disease:IMD - Gaucher disease
Specific disease:IMD - Hunter syndrome
Specific disease:IMD - Krabbe disease
Specific disease:IMD - Metachromatic leukodystrophy (MLD)
Specific disease:IMD - Mannosidosis
Specific disease:IMD - Not otherwise specified
Specific disease:IMD - Neimann - Pick disease
Specific disease:IMD - Osteopetrosis
Specific disease:IMD - Hurler syndrome (mps-ih or mps i)
Specific disease:IMD - Mucopolysaccharidosis (V)
Specific disease:IMD - Mucopolysaccharidosis, not otherwise specified
Specific disease:IMD - Neuronal ceriod - lipofuscinosis (Batten disease)
Specific disease:IMD - Sanfilippo (III)
Specific disease:IMD - Morquio (IV)
Specific disease:IPA - Glanzmann thrombasthenia
Specific disease:IPA - Other inherited platelet abnormality
Specific disease:IPA - Congenital amegakaryocytosis/congenital thrombocytopenia
Specific disease:MDS - 5q minus syndrome
Specific disease:MDS - MDS with excess blasts-1
Specific disease:MDS - MDS with excess blasts-2
Specific disease:MDS/MPN - Chronic myelomonocytic leukemia
Specific disease:MDS/MPN - Atypical chronic myeloid leukemia
Specific disease:MDS/MPN - Juvenile chronic myelomonocytic leukemia
Specific disease:MDS - MDS / MPN with ring sideroblasts and thrombocytosis (MDS / MPN-RS-T)
Specific disease:MDS - Mastocytosis
Specific disease:MDS - Not otherwise specified
Specific disease:MDS - Refractory anemia with ringed sideroblasts
Specific disease:MDS - Refractory cytopenia with unilineage dysplasia (RCUD) includes refractory anemia (RA)
Specific disease:MDS - MDS-RS with multilineage dysplasia
Specific disease:MDS - MDS-RS with single lineage dysplasia
Specific disease:MDS - Atypical chronic myeloid leukemia (aCML), BCR-ABL1-
Specific disease:MDS - Myelodysplastic syndrome with multilineage dysplasia
Specific disease:MDS - Myeloid / lymphoid neoplasms with FGFR1 rearrangement
Specific disease:MDS - Myeloid / lymphoid neoplasms with PCM1-JAK2
Specific disease:MDS - Myeloid / lymphoid neoplasms with PDGFRB rearrangement
Specific disease:MDS - Refractory cytopenia of childhood
Specific disease:MDS - Myelodysplastic syndrome with single lineage dysplasia
Specific disease:MM - Multiple myeloma-IgM (not Waldenstrom macroglobulinemia)
Specific disease:MM - Multiple myeloma, Not otherwise specified
Specific disease:MM - Smoldering myeloma
Specific disease:MM - Multiple myeloma-IgA
Specific disease:MM - Multiple myeloma-IgD
Specific disease:MM - Multiple myeloma-IgE
Specific disease:MM - Multiple myeloma-IgG
Specific disease:MM - Multiple myeloma-light chain only
Specific disease:MM - Multiple myeloma-Multiple Chain
Specific disease:MM - Multiple myeloma-non-secretory
Specific disease:MPN - Systemic mastocytosis
Specific disease:MPN - Chronic eosinophilic leukemia (hypereosinophilic syndrome)
Specific disease:MPN - Chronic neutrophilic leukemia
Specific disease:MPN - Essential thrombocythemia
Specific disease:MPN - Polycythemia vera
Specific disease:MPN - Primary myelofibrosis
Specific disease:MPN - Post-essential thrombocythemic myelofibrosis
Specific disease:MPN - Post-polycythemic myelofibrosis
Specific disease:MPN - Myeloproliferative neoplasm (MPN), unclassifiable
Specific disease:NHL - Anaplastic large-cell lymphoma (ALCL), ALK negative
Specific disease:NHL - Anaplastic large-cell lymphoma (ALCL), ALK positive
Specific disease:NHL - Burkitt lymphoma
Specific disease:NHL - Diffuse, large B-cell lymphoma- Germinal center B-cell type
Specific disease:NHL - DLBCL associated with chronic inflammation
Specific disease:NHL - Diffuse, large B-cell lymphoma- Activated B-cell type (non-GCB)
Specific disease:NHL - Diffuse, Large B-cell Lymphoma (cell of origin unknown)
Specific disease:NHL - EBV+ DLBCL, NOS
Specific disease:NHL - EBV+ mucocutaneous ulcer
Specific disease:NHL - Follicular T-cell lymphoma
Specific disease:NHL - HHV8+ DLBCL, NOS
Specific disease:NHL - Hepatosplenic T-cell lymphoma
Specific disease:NHL - Lymphomatoid granulomatosis
Specific disease:NHL - Mantle cell lymphoma
Specific disease:NHL - Mycosis fungoides
Specific disease:NHL - Plasmablastic lymphoma
Specific disease:NHL - Plasmacytic hyperplasia PTLD
Specific disease:NHL - Primary CNS lymphoma
Specific disease:NHL - Primary effusion lymphoma
Specific disease:NHL - Sezary syndrome
Specific disease:NHL - Subcutaneous panniculitis-like T-cell lymphoma
Specific disease:NHL - Systemic EBV+ T-cell lymphoma of childhood
Specific disease:NHL - Adult T-cell lymphoma/leukemia
Specific disease:NHL - Aggressive NK-cell leukemia
Specific disease:NHL - Angioimmunoblastic T-cell lymphoma
Specific disease:NHL - Breast implant-associated anaplastic large-cell lymphoma
Specific disease:NHL - Chronic lymphoproliferative disorder of NK cells
Specific disease:NHL - Primary cutaneous CD30+ T-cell lymphoproliferative disorders
Specific disease:NHL - Primary cutaneous DLBCL, leg type
Specific disease:NHL - Primary cutaneous CD8+ aggressive epidermotropic cytotoxic T-cell lymphoma
Specific disease:NHL - Primary cutaneous follicle center lymphoma
Specific disease:NHL - Primary cutaneous gamma-delta T-cell lymphoma
Specific disease:NHL - Primary cutaneous CD4+ small / medium T-cell lymphoproliferative disorder
Specific disease:NHL - Enteropathy-type T-cell lymphoma
Specific disease:NHL - Extranodal marginal zone B-cell lymphoma of mucosal associated lymphoid tissue type
Specific disease:NHL - Extranodal NK / T-cell lymphoma, nasal type
Specific disease:NHL - Follicular, predominantly small cleaved cell (Grade I follicle center lymphoma)
Specific disease:NHL - Follicular, mixed, small cleaved and large cell (Grade II follicle center lymphoma)
Specific disease:NHL - Follicular, predominantly large cell (Grade IIIA follicle center lymphoma)
Specific disease:NHL - Follicular, predominantly large cell (Grade IIIB follicle center lymphoma)
Specific disease:NHL - Follicular, predominantly large cell (Grade IIIA vs IIIB not specified)
Specific disease:NHL - Follicular (grade unknown)
Specific disease:NHL - High-grade B-cell lymphoma, with MYC and BCL2 and/or BCL6 rearrangements
Specific disease:NHL - High-grade B-cell lymphoma, NOS
Specific disease:NHL - Indolent T-cell lymphoproliferative disorder of the GI tract
Specific disease:NHL - With features intermediate between DLBCL and classic Hodgkin Lymphoma
Specific disease:NHL - Intravascular large B-cell lymphoma
Specific disease:NHL - Large B-cell lymphoma with IRF4 rearrangement
Specific disease:NHL - ALK+ large B-cell lymphoma
Specific disease:NHL - T-cell large granular lymphocytic leukemia
Specific disease:NHL - Lymphoplasmacytic lymphoma/ Waldenstrom macroglobulinemia
Specific disease:NHL - Monomorphic epitheliotropic intestinal T-cell lymphoma
Specific disease:NHL - Monomorphic PTLD (B- and T-/NK-cell types)
Specific disease:NHL - Nodal peripheral T-cell lymphoma with TFH phenotype
Specific disease:NHL - Nodal marginal zone B-cell lymphoma
Specific disease:NHL - Other B-cell lymphoma
Specific disease:NHL - Other T-cell/NK-cell lymphoma
Specific disease:NHL - Peripheral T-cell lymphoma (PTCL), NOS
Specific disease:NHL - Polymorphic PTLD
Specific disease:NHL - Splenic diffuse red pulp small B-cell lymphoma
Specific disease:NHL - Splenic marginal zone B-cell lymphoma
Specific disease:NHL - T-cell / histiocytic rich large B-cell lymphoma
Specific disease:NHL - Primary mediastinal (thymic) large B-cell lymphoma
Specific disease:OAL - Biphenotypic leukemia
Specific disease:OAL - Mixed phenotype acute leukemia (MPAL) with t(9;22)(q34.1;q11.2); BCR-ABL1
Specific disease:OAL - Not otherwise specified
Specific disease:OAL - Blastic plasmacytoid dendtritic cell neoplasm
Specific disease:OAL - Mixed phenotype acute leukemia, B/myeloid, NOS
Specific disease:OAL - Mixed phenotype acute leukemia, T/myeloid, NOS
Specific disease:OND - Not otherwise specified
Specific disease:OTH_LEUK - CLL, not otherwise specified
Specific disease:OTH_LEUK - CLL, B-cell / small lymphocytic lymphoma
Specific disease:OTH_LEUK - Not otherwise specified
Specific disease:OTH_LEUK - Prolymphocytic Leukemia (PLL)
Specific disease:PCD - Amyloidosis
Specific disease:PCD - Monoclonal gammopathy of renal significance (MGRS)
Specific disease:PCD - Not otherwise specified
Specific disease:PCD - Osteosclerotic myeloma / POEMS syndrome
Specific disease:PCD - Plasma cell leukemia
Specific disease:PCD - Solitary plasmacytoma
Specific disease:PNH - Paroxysmal nocturnal hemoglobinuria
Specific disease:STU - Bone sarcoma (excluding Ewing family tumors)
Specific disease:STU - Central nervous system tumor
Specific disease:STU - Ewing family tumors of bone (includes PNET)
Specific disease:STU - Ewing family tumors extra-osseous (includes PNET)
Specific disease:STU - External genitalia (Penile)
Specific disease:STU - Germ cell tumors
Specific disease:STU - Head and neck cancer
Specific disease:STU - Mediastinal neoplasm
Specific disease:STU - Medulloblastoma
Specific disease:STU - Melanoma
Specific disease:STU - Not otherwise specified
Specific disease:STU - Neuroblastoma
Specific disease:STU - Neurogenic sarcoma
Specific disease:STU - Ovary
Specific disease:STU - Pancreatic
Specific disease:STU - Prostate
Specific disease:STU - Retinoblastoma
Specific disease:STU - Rhabdomyosarcoma
Specific disease:STU - Soft tissue sarcoma
Specific disease:STU - Testicular
Specific disease:STU - Wilm tumor
Specific disease:STU - Synovial sarcoma
Female
Male
2016 transplant year
2017 transplant year
2018 transplant year
2019 transplant year
2020 transplant year