Center name
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 75 years old
Bone marrow
Cord blood
Peripheral blood stem cells
HSCT
Disease category: Autoimmune disease (AI)
Disease category: Acute lymphoblastic leukemia (ALL)
Disease category: Acute myeloid leukemia (AML)
Disease category: Aplastic Anemia (AA)
Disease category: Chronic myeloid 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: 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: Other plasma cell disease (PCD)
Disease category: Paroxysmal nocturnal hemoglobinuria (PNH)
Disease cateogry: Recessive dystrophic epidermolysis bullosa (RDEB)
Disease category: Solid tumors (STU)
Disease cateogry: Tolerance induction associated with solid organ transplant (TIASOT)
1st Remission
2nd or subsequent remission
Data unavailable
In remission
Not applicable
Not in remission
Autologous
HLA-matching sibling
Other related donor
Unrelated
Hispanic or Latino
Not Hispanic or Latino
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: Acquired AA, not otherwise specified
Specific disease on form: Other acquired cytopenic syndrome
Specific disease on form: Acquried AA secondary to chemotherapy
Specific disease on form: Acquired AA secondary to immunotherapy or immune effector cell therapy
Specific disease on form: Acquired AA, secondary to hepatitis
Specific disease on form: Behcet Syndrome
Specific disease on form: Crohn's disease
Specific disease on form: Evans syndrome
Specific disease on form: Hemolytic anemia
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: Juvenile idiopathic arthritis (JIA): polyarticular
Specific disease on form: Juvenile idiopathic arthritis (JIA): systemic (Still's disease)
Specific disease on form: Myasthenia gravis
Specific disease on form: Other autoimmune disorder
Specific disease on form: Systemic sclerosis
Specific disease on form: Early T-precursor lymphoblastic leukemia / lymphoma
Specific disease on form: ALL, not otherwise specified
Specific disease on form: B-lymphoblastic leukemia / lymphoma, BCR::ABL1-like features
Specific disease on form: B-lymphoblastic leukemia / lymphoma with ETV6::RUNX1 fusion
Specific disease on form: B-lymphoblastic leukemia / lymphoma with hypodiploidy
Specific disease on form: B-lymphoblastic leukemia / lymphoma with IGH::IL3 fusion
Specific disease on form: B-lymphoblastic leukemia / lymphoma with KMT2A rearrangement
Specific disease on form: B-lymphoblastic leukemia / lymphoma, not otherwise specified
Specific disease on form: B-lymphoblastic leukemia / lymphoma with TCF3::PBX1 fusion
Specific disease on form: B-lymphoblastic leukemia / lymphoma with high hyperdiploidy
Specific disease on form: B-lymphoblastic leukemia / lymphoma, with iAMP21
Specific disease on form: T-lymphoblastic leukemia / lymphoma
Specific disease on form: Acute promyelocytic leukemia with PML::RARA fusion
Specific disease on form: Acute erythroid leukemia
Specific disease on form: Transformed to AML
Specific disease on form: Acute megakaryoblastic leukemia
Specific disease on form: Acute monocytic leukemia
Specific disease on form: Acute myelomonocytic leukemia
Specific disease on form: Acute panmyelosis with myelofibrosis
Specific disease on form: Acute myeloid leukemia with BCR::ABL1 fusion
Specific disease on form: Acute myeloid leukemia with CBFB::MYH11 fusion
Specific disease on form: Acute myeloid leukemia with CEBPA mutation
Specific disease on form: Acute myeloid leukemia with DEK::NUP214 fusion
Specific disease on form: Acute myeloid leukemia with MECOM (EVI1), GATA2 rearrangement
Specific disease on form: Acute myeloid leukemia with MLLT3::KMT2A fusion
Specific disease on form: Myeloid sarcoma
Specific disease on form: Acute myeloid leukemia, not otherwise specified
Specific disease on form: Acute myeloid leukemia with NPM1 mutation
Specific disease on form: Acute myeloid leukemia with NUP98 rearrangement
Specific disease on form: Acute myeloid leukemia without maturation
Specific disease on form: Acute myeloid leukemia with RBM15::MRTFA fusion
Specific disease on form: AML with mutated RUNX1 (provisional entity)
Specific disease on form: Acute myeloid leukemia with RUNX1::RUNX1T1 fusion
Specific disease on form: Acute myeloid leukemia with mutated TP53
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: Acute myeloid leukemia with maturation
Specific disease on form: Acute myeloid leukemia with minimal differentiation
Specific disease on form: Acute myeloid leukemia with myelodysplasia - related
Specific disease on form: Acute myeloid leukemia with other KMT2A rearrangements
Specific disease on form: Acute myeloid leukemia with other defined genetic alterations
Specific disease on form: Ph1+; BCR/ABL+
Specific disease on form: Ph1 unknown; BCR/ABL+
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
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: Classic Hodgkin lymphoma
Specific disease on form: Hodgkin lymphoma: lymphocyte depleted
Specific disease on form: Lymphocyte-rich
Specific disease on form: Hodgkin lymphoma: mixed cellularity
Specific disease on form: Nodular lymphocyte predominant Hodgkin lymphoma
Specific disease on form: Hodgkin lymphoma: nodular sclerosis
Specific disease on form: Telomere Biology Disorders including Dyskeratosis congenita (DKC1, TERT, TERC, and other mutations)
frm_IBMFS_Diamond_blackfan_anemia
Specific disease on form: Fanconi anemia
Specific disease on form: Severe congenital neutropenia
Specific disease on form: Shwachman-Diamond anemia
Specific disease on form: Other inherited bone marrow failure syndrome
Specific disease on form: Wolman disease
Specific disease on form: Other constitutional anemia
Specific disease on form: Ataxia telangiectasia
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: Leukocyte adhesion deficiencies
Specific disease on form: MHC Class II Deficiency (Bare Lymphocyte Syndrome)
Specific disease on form: NEMO Deficiency Syndrome
Specific disease on form: Omenn syndrome
Specific disease on form: Other immunodeficiencies
Specific disease on form: Other SCID
Specific disease on form: SAP Deficiency (XIAP-1)
Specific disease on form: SCID, T- B- NK-, Adenosine deaminase (ADA) deficiency
Specific disease on form: SCID, not otherwise specified
Specific disease on form: Absence of T and B cells SCID
Specific disease on form: SCID,T- B+ NK+, ILR alpha deficiency
frm_IIS_SCID_reticular_dysgenesis
Specific disease on form: STAT1 Gain of Function
Specific disease on form: Wiskott-Aldrich syndrome
Specific disease on form: DiGeorge anomaly
Specific disease on form: Immune deficiency, not otherwise specified
Specific disease on form: Adrenoleukodystrophy (ALD)
Specific disease on form: Fucosidosis
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: Mucopolysaccharidosis, not otherwise specified
Specific disease on form: Mannosidosis
Specific disease on form: Morquio (IV)
Specific disease on form: Inherited metabolic disorder, not otherwise specified
Specific disease on form: Niemann-Pick 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 (501)
Specific disease on form: Glanzmann thrombasthenia (502)
Specific disease on form: Other inherited platelet abnormality (509)
Specific disease on form: Chronic myelomonocytic leukemia (CMML), Myelodysplastic
Specific disease on form: Chronic myelomonocytic leukemia (CMML), Myeloproliferative
Specific disease on form: Myelodysplastic syndrome with increased blasts (MDS-IB1)
Specific disease on form: Myelodysplastic syndrome with increased blasts (MDS-IB2)
Specific disease on form: Myelodysplastic syndrome / myeloproliferative neoplasm, not otherwise specified
Specific disease on form: Myelodysplastic/myeloproliferative neoplasm with neutrophilia
Specific disease on form: Mastocytosis
Specific disease on form: RARS
Specific disease on form: MDS-RS with multilineage dysplasia
Specific disease on form: Myelodysplastic/myeloproliferative neoplasm with SF3B1 mutation and thrombocytosis (MDS / MPNâ€“RSâ€“T)
Specific disease on form: MDS unclassifiable, not otherwise specified
Specific disease on form: Myelodysplastic syndrome with biallelic TP53 inactivation (MDS-biTP53)
Specific disease on form: Childhood MDS with low blasts, hypocellular
Specific disease on form: Myelodysplastic syndrome, hypoplastic (MDS-h) &le;25% cellularity by age
Specific disease on form: Juvenile myelomonocytic leukemia (JMML)
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: Myelodysplastic syndrome with low blasts (MDS-LB; <5% BM, <2%PB)
Specific disease on form: Myelodysplastic syndrome with low blasts and isolated 5q deletion (MDS-5q)
Specific disease on form: Multiple myeloma-light chain only
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-IgG
Specific disease on form: Multiple myeloma-Multiple Chain
Specific disease on form: Chronic eosinophilic leukemia, not otherwise specified
Specific disease on form: Chronic neutrophilic leukemia
Specific disease on form: Essential thrombocythemia
Specific disease on form: Mast cell sarcoma (MCS)
Specific disease on form: Polycythemia vera (PCV)
Specific disease on form: Primary myelofibrosis (PMF)
Specific disease on form: Post-essential thrombocythemic myelofibrosis
Specific disease on form: Post-polycythemic myelofibrosis
Specific disease on form: Myeloproliferative neoplasm (MPN), unclassifiable
Specific disease on form: Myeloid / lymphoid neoplasms with PDGFRA rearrangement
Specific disease on form: Systemic mastocytosis
Specific disease on form: ALK-negative anaplastic large-cell lymphoma
Specific disease on form: ALK-positive anaplastic large cell lymphoma
Specific disease on form: Adult T-cell lymphoma / leukemia
Specific disease on form: Aggressive NK-cell leukemia
Specific disease on form: Breast implant-associated anaplastic large cell lymphoma
Specific disease on form: Burkitt lymphoma
Specific disease on form: Classical Hodgkin lymphoma PTLD
Specific disease on form: Primary cutaneous CD8-positive aggressive epidermotropic cytotoxic T-cell lymphoma
Specific disease on form: Primary cutaneous diffuse large B-cell lymphoma, leg type
Specific disease on form: Primary large B-cell lymphoma of the CNS
Specific disease on form: Primary cutaneous gamma / delta T-cell lymphoma
Specific disease on form: Diffuse large B-cell lymphoma - Germinal Center B-cell subtype
Specific disease on form: Diffuse large B-cell lymphoma, not otherwise specified
Specific disease on form: Diffuse large B-cell lymphoma - Activated B-cell type subtype
Specific disease on form: Diffuse large B-cell lymphoma associated with chronic inflammation
Specific disease on form: Diffuse large B-cell lymphoma / high-grade B-cell lymphoma with MYC and BCL2 rearrangements
Specific disease on form: Diffuse large B-cell lymphoma / high grade B-cell lymphoma with MYC and BCL6 rearrangements
Specific disease on form: EBV-positive diffuse large B-cell lymphoma
Specific disease on form: Enteropathy-associated T-cell lymphoma
Specific disease on form: Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue
Specific disease on form: Follicular, predominantly small cleaved cell (Grade I follicle center lymphoma)
Specific disease on form: Follicular, mixed, small cleaved and large cell (Grade II follicle center lymphoma)
Specific disease on form: Follicular (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: Hepatosplenic T-cell lymphoma
Specific disease on form: High-grade B-cell lymphoma, not otherwise specified
Specific disease on form: Intravascular large B-cell lymphoma
Specific disease on form: KSHV / HHV8-positive diffuse large B-cell lymphoma
Specific disease on form: Large B-cell lymphoma with IRF4 rearrangement
Specific disease on form: ALK-positive large B-cell lymphoma
Specific disease on form: T-cell / histiocytic-rich large B-cell lymphoma
Specific disease on form: T-large granular lymphocytic leukemia
Specific disease on form: Lymphoplasmacytic lymphoma
Specific disease on form: Lymphomatoid granulomatosis
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 TFH cell lymphoma, not otherwise specified
Specific disease on form: Nodal TFH cell lymphoma, angioimmunoblastic-type
Specific disease on form: Nodal TFH cell lymphoma, follicular-type
Specific disease on form: Nodal marginal zone lymphoma
Specific disease on form: Other B-cell lymphoma
Specific disease on form: Peripheral T-cell lymphoma, not otherwise specified
Specific disease on form: Plasmablastic lymphoma
Specific disease on form: Primary effusion lymphoma
Specific disease on form: Primary mediastinal large B-cell lymphoma
Specific disease on form: Sézary syndrome
Specific disease on form: Splenic marginal zone 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: Primary cutaneous CD30-positive T-cell lymphoproliferative disorder: Lymphomatoid papulosis
Specific disease on form: Primary cutaneous follicle center lymphoma
Specific disease on form: Primary cutaneous CD4-positive small or medium T-cell lymphoproliferative disorder
Specific disease on form: Splenic diffuse red pulp small B-cell lymphoma
Specific disease on form: Extranodal NK / T-cell lymphoma
Specific disease on form: Hyperplasia arising in immune deficiencies (e.g. PTLD)
Specific disease on form: Mediastinal grey zone lymphoma
Specific disease on form: Other T-cell / NK-cell lymphoma
Specific disease on form: Polymorphic lymphoproliferative disorders arising in immune deficiency / dysregulation
Specific disease on form: Indolent T-cell lymphoma of the gastrointestinal tract
Specific disease on form: Acute leukemia of ambiguous lineage, not otherwise specified
Specific disease on form: Biphenotypic, bilineage or hybrid leukemia
Specific disease on form: Mixed-phenotype acute leukemia, B/myeloid
Specific disease on form: Mixed phenotype acute leukemia with KMT2A rearrangement
Specific disease on form: Mixed-phenotype acute leukemia, T/myeloid
Specific disease on form: Mixed phenotype acute leukemia (MPAL) with BCR::ABL1 fusion
Specific disease on form: Acute undifferentiated leukemia
Specific disease on form: Other leukemia
Specific disease on form: Chronic lymphocytic leukemia (CLL), not otherwise specified
Specific disease on form: Chronic lymphocytic leukemia / small lymphocytic lymphoma
Specific disease on form: Hairy cell leukemia
Specific disease on form: Prolymphocytic Leukemia (PLL), not otherwise specified
Specific disease on form: PLL, B-cell
Specific disease on form: Other leukemia, not otherwise specified
Specific disease on form: Other plasma cell disorder
Specific disease on form: T-prolymphocytic leukemia
Specific disease on form: Immuno-globulin-related (AL) amyloidosis
Specific disease on form: Monoclonal gammopathy of renal significance (MGRS)
Specific disease on form: Multiple myeloma
Specific disease on form: IgD (heavy chain only)
Specific disease on form: IgD kappa
Specific disease on form: IgD lambda
Specific disease on form: IgE kappa
Specific disease on form: IgE lambda
Specific disease on form: IgG (heavy chain only)
Specific disease on form: IgG kappa
Specific disease on form: IgG lambda
Specific disease on form: IgM (heavy chain only)
Specific disease on form: IgM kappa
Specific disease on form: IgM lambda
Specific disease on form: Kappa (light chain only)
Specific disease on form: Lambda (light chain only)
Specific disease on form: IgA (heavy chain only)
Specific disease on form: IgA kappa
Specific disease on form: IgA lambda
Specific disease on form: POEMS syndrome
Specific disease on form: Plasma cell leukemia
Specific disease on form: Plasmacytoma
Specific disease on form: Paroxysmal nocturnal hemoglobinuria
Specific disease on form: Recessive dystrophic epidermolysis bullosa
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 of tumors of bone (including PNET)
Specific disease on form: Ewing family of tumors, extraosseous (including PNET)
Specific disease on form: Germ cell tumor, extragonadal
Specific disease on form: Germ cell tumors, gonadal
Specific disease on form: Malignant Peripheral Nerve Sheath Tumor
Specific disease on form: Mediastinal neoplasm
Specific disease on form: Medulloblastoma
Specific disease on form: Solid tumor, not otherwise specified
Specific disease on form: Neuroblastoma
Specific disease on form: Other solid tumor
Specific disease on form: Ovarian (epithelial)
Specific disease on form: Pancreatic cancer
Specific disease on form: Renal cell
Specific disease on form: Retinoblastoma
Specific disease on form: Rhabdomyosarcoma
Specific disease on form: Testicular cancer
Specific disease on form: Tumors of the head / neck
Specific disease on form: Wilm's tumor
Specific disease on form: Other Soft tissue sarcoma (excluding Ewing family tumors)
Specific disease on form: Synovial sarcoma
Specific disease on form: Lung, not otherwise specified
Specific disease on form: Unknown
American Indian or Alaska Native
Asian
Black or African American
Native Hawaiian or other Pacific Islander
Multiple races
White
Specific disease: AA - Acquired AA, secondary to hepatitis
Specific disease: AA - Acquired pure red cell aplasia
Specific disease: AA - Acquired AA, secondary to toxin / other drug
Specific disease: AA - Amegakaryocytosis (not congenital)
Specific disease: AA - Aplastic anemia
Specific disease: AA - Acquired AA, not otherwise specified
Specific disease: AI - Crohn's disease
Specific disease: AI - Hemolytic anemia
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 (JIA): polyarticular
Specific disease: AI - Juvenile idiopathic arthritis (JIA): systemic (Still's 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 - Systemic sclerosis
Specific disease: ALL - Early T-precursor lymphoblastic leukemia / lymphoma
Specific disease: ALL - Not otherwise specified
Specific disease: ALL - B-lymphoblastic leukemia / lymphoma with BCR::ABL1 fusion
Specific disease: ALL - B-lymphoblastic leukemia / lymphoma, BCR::ABL1-like features
Specific disease: ALL - B-lymphoblastic leukemia / lymphoma with ETV6::RUNX1 fusion
Specific disease: ALL - B-lymphoblastic leukemia / lymphoma with IGH::IL3 fusion
Specific disease: ALL - B-lymphoblastic leukemia / lymphoma with KMT2A rearrangement
Specific disease: ALL - B-lymphoblastic leukemia / lymphoma, not otherwise specified
Specific disease: ALL - B-lymphoblastic leukemia / lymphoma with TCF3::PBX1 fusion
Specific disease: ALL - B-lymphoblastic leukemia / lymphoma with hypodiploidy
Specific disease: ALL - B-lymphoblastic leukemia / lymphoma, with iAMP21
Specific disease: ALL - Natural killer (NK)- cell lymphoblastic leukemia / lymphoma
Specific disease: ALL - T-lymphoblastic leukemia / lymphoma
Specific disease: AML - Acute promyelocytic leukemia with PML::RARA fusion
Specific disease: AML - Transformed to AML
Specific disease: AML - Acute myelomonocytic leukemia
Specific disease: AML - Acute myeloid leukemia with BCR::ABL1 fusion
Specific disease: AML - Acute myeloid leukemia with CBFB::MYH11 fusion
Specific disease: AML - Acute myeloid leukemia with CEBPA mutation
Specific disease: AML - Acute myeloid leukemia with DEK::NUP214 fusion
Specific disease: AML - Acute myeloid leukemia with MECOM (EVI1), GATA2 rearrangement
Specific disease: AML - Acute panmyelosis with myelofibrosis
Specific disease: AML - Acute myeloid leukemia with MLLT3::KMT2A fusion
Specific disease: AML - Myeloid sarcoma
Specific disease: AML - Acute myeloid leukemia with NPM1 mutation
Specific disease: AML - Acute myeloid leukemia, not otherwise specified
Specific disease: AML - Acute myeloid leukemia with NUP98 rearrangement
Specific disease: AML - Acute myeloid leukemia without maturation
Specific disease: AML - Acute myeloid leukemia with RBM15::MRTFA fusion
Specific disease: AML - Acute myeloid leukemia with mutated RUNX1 (provisional entity)
Specific disease: AML - Acute myeloid leukemia with RUNX1::RUNX1T1 fusion
Specific disease: AML - Acute myeloid leukemia with mutated TP53
Specific disease: AML - Therapy related AML (t-AML)
Specific disease: AML - Acute erythroid leukemia
Specific disease: AML - Acute megakaryoblastic leukemia
Specific disease: AML - Acute monocytic leukemia
Specific disease: AML - Myeloid leukemia associated with Down syndrome
Specific disease: AML - Acute myeloid leukemia with maturation
Specific disease: AML - Acute myeloid leukemia with minimal differentiation
Specific disease: AML - Acute myeloid leukemia with myelodysplasia - related
Specific disease: AML - Acute myeloid leukemia with other KMT2A rearrangements
Specific disease: AML - Acute myeloid leukemia with other defined genetic alterations
Specific disease: AI - Behcet syndrome
Specific disease: CML - Chronic Myeloid Leukemia
Specific disease: AI - Evans syndrome
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 - Classic Hodgkin lymphoma
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 - Nodular sclerosis
Specific disease: HL - Nodular lymphocyte predominant
Specific disease: IBMFS - Telomere Biology Disorders including Dyskeratosis congenita (DKC1, TERT, TERC, and other mutations)
Specific disease: IBMFS - Fanconi anemia
Specific disease: IBMFS - Severe congenital neutropenia
Specific disease: IBMFS - Shwachmann-Diamond syndrome
Specific disease: IBMFS - Other inherited bone marrow failure syndrome
Specific disease: IEA - Other constitutional anemia
Specific disease: IIS - Ataxia telangiectasia
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 - Immune deficiency
Specific disease: IIS - Leukocyte adhesion deficiencies
Specific disease: IIS - MHC Class II Deficiency (Bare Lymphocyte Syndrome)
Specific disease: IIS - NEMO Deficiency Syndrome
Specific disease: IIS - Not otherwise specified
Specific disease: IIS - Omenn syndrome
Specific disease: IIS - SAP Deficiency (XIAP-1)
Specific disease: IIS - Severe combined immunodeficiency (SCID)
Specific disease: IIS - SCID, T- B- NK-, Adenosine deaminase (ADA) deficiency
Specific disease: IIS - SCID, T- B- NK-, Reticular dysgenesis
Specific disease: IIS - SCID,T- B+ NK+, ILR alpha deficiency
Specific disease: IIS - STAT1 Gain of Function
Specific disease: IIS - Wiskott-Aldrich syndrome (WAS)
Specific disease: IIS - DiGeorge anomaly
Specific disease: IMD - Adrenoleukodystrophy (ALD)
Specific disease: IMD - Fucosidosis
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 - Niemann-Pick disease
Specific disease: IMD - Osteopetrosis
Specific disease: IMD - Hurler syndrome (MPS-IH or MPS-I)
Specific disease: IMD - Mucopolysaccharidosis, not otherwise specified
Specific disease: IMD - Neuronal ceroid lipofuscinosis (Batten disease)
Specific disease: IMD - Sanfilippo (III)
Specific disease: IMD - Wolman disease
Specific disease: IMD - Morquio (IV)
Specific disease: IPA - Congenital amegakaryocytosis / congenital thrombocytopenia
Specific disease: IPA - Glanzmann thrombasthenia
Specific disease: IPA - Other inherited platelet abnormality
Specific disease: MDS - Chronic myelomonocytic leukemia (CMML), Myelodysplastic
Specific disease: MDS - Chronic myelomonocytic leukemia (CMML), Myeloproliferative
Specific disease: MDS - Myelodysplastic syndrome with increased blasts (MDS-IB1)
Specific disease: MDS - Myelodysplastic syndrome with increased blasts (MDS-IB2)
Specific disease: MDS - Myelodysplastic syndrome / myeloproliferative neoplasm, not otherwise specified
Specific disease: MDS - Myelodysplastic/myeloproliferative neoplasm with neutrophilia
Specific disease: MDS - Mastocytosis
Specific disease: MDS - Not otherwise specified
Specific disease: MDS - Refractory anemia with ringed sideroblasts
Specific disease: MDS - MDS-RS with multilineage dysplasia
Specific disease: MDS - MDS-RS with single lineage dysplasia
Specific disease: MDS - Myelodysplastic/myeloproliferative neoplasm with SF3B1 mutation and thrombocytosis (MDS / MPNâ€“RSâ€“T)
Specific disease: MDS - Myelodysplastic syndrome with biallelic TP53 inactivation (MDS-biTP53)
Specific disease: MDS - Childhood MDS with low blasts, hypocellular
Specific disease: MDS - Myelodysplastic syndrome, hypoplastic (MDS-h) <=25% cellularity by age
Specific disease: MDS - Juvenile myelomonocytic leukemia (JMML)
Specific disease: MDS - Myelodysplastic syndrome with multilineage dysplasia
Specific disease: MDS - Myelodysplastic syndrome with single lineage dysplasia
Specific disease: MDS - Myelodysplastic syndrome with low blasts (MDS-LB; <5% BM, <2% PB)
Specific disease: MDS - Myelodysplastic syndrome with low blasts and isolated 5q deletion (MDS-5q)
Specific disease: MM - Multiple myeloma-light chain only
Specific disease: PCD - Multiple myeloma-Multiple Chain
Specific disease: PCD - Multiple myeloma-non-secretory
Specific disease: MPN - Systemic mastocytosis
Specific disease: MPN - Chronic eosinophilic leukemia, not otherwise specified
Specific disease: MPN - Chronic neutrophilic leukemia
Specific disease: MPN - Essential thrombocythemia
Specific disease: MPN - Mast cell sarcoma (MCS)
Specific disease: MPN - Polycythemia vera (PCV)
Specific disease: MPN - Primary myelofibrosis (PMF)
Specific disease: MPN - Myeloid / lymphoid neoplasms with FGFR1 rearrangement
Specific disease: MPN - Myeloid / lymphoid neoplasms with PCM1-JAK2
Specific disease: MPN - Myeloid / lymphoid neoplasms with PDGFRA rearrangement
Specific disease: MPN - Myeloid / lymphoid neoplasms with PDGFRB rearrangement
Specific disease: MPN - Post-essential thrombocythemic myelofibrosis
Specific disease: MPN - Post-polycythemic myelofibrosis
Specific disease: MPN - Myeloproliferative neoplasm (MPN), unclassifiable
Specific disease: NHL - ALK-negative anaplastic large-cell lymphoma
Specific disease: NHL - ALK-positive anaplastic large cell lymphoma
Specific disease: NHL - Adult T-cell lymphoma / leukemia
Specific disease: NHL - Breast implant-associated anaplastic large cell lymphoma
Specific disease: NHL - Burkitt lymphoma
Specific disease: NHL - Primary cutaneous CD8-positive aggressive epidermotropic cytotoxic T-cell lymphoma
Specific disease: NHL - Primary cutaneous diffuse large B-cell lymphoma, leg type
Specific disease: NHL - Primary large B-cell lymphoma of the CNS
Specific disease: NHL - Primary cutaneous gamma / delta T-cell lymphoma
Specific disease: NHL - Diffuse large B-cell lymphoma - Germinal Center B-cell subtype
Specific disease: NHL - Diffuse large B-cell lymphoma, not otherwise specified
Specific disease: NHL - Diffuse large B-cell lymphoma - Activated B-cell type subtype
Specific disease: NHL - Diffuse large B-cell lymphoma associated with chronic inflammation
Specific disease: NHL - Diffuse large B-cell lymphoma / high-grade B-cell lymphoma with MYC and BCL2 rearrangements
Specific disease: NHL - Diffuse large B-cell lymphoma / high grade B-cell lymphoma with MYC and BCL6 rearrangements
Specific disease: NHL - EBV-positive diffuse large B-cell lymphoma
Specific disease: NHL - Enteropathy-associated T-cell lymphoma
Specific disease: NHL - Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue
Specific disease: NHL - Hepatosplenic T-cell lymphoma
Specific disease: NHL - High-grade B-cell lymphoma, not otherwise specified
Specific disease: NHL - KSHV / HHV8-positive diffuse large B-cell lymphoma
Specific disease: NHL - ALK-positive large B-cell lymphoma
Specific disease: NHL - T-cell / histiocytic-rich large B-cell lymphoma
Specific disease: NHL - T-large granular lymphocytic leukemia
Specific disease: NHL - Lymphomatoid granulomatosis
Specific disease: NHL - Lymphoplasmacytic lymphoma
Specific disease: NHL - Mantle cell lymphoma
Specific disease: NHL - Mycosis fungoides
Specific disease: NHL - Nodal TFH cell lymphoma, not otherwise specified
Specific disease: NHL - Nodal TFH cell lymphoma, angioimmunoblastic-type
Specific disease: NHL - Nodal TFH cell lymphoma, follicular-type
Specific disease: NHL - Nodal marginal zone lymphoma
Specific disease: NHL - Peripheral T-cell lymphoma, not otherwise specified
Specific disease: NHL - Plasmablastic lymphoma
Specific disease: NHL - Primary mediastinal large B-cell lymphoma
Specific disease: NHL - Primary effusion lymphoma
Specific disease: NHL - Sézary syndrome
Specific disease: NHL - Splenic marginal zone lymphoma
Specific disease: NHL - Subcutaneous panniculitis-like T-cell lymphoma
Specific disease: NHL - Systemic EBV+ T-cell lymphoma of childhood
Specific disease: NHL - Aggressive NK-cell leukemia
Specific disease: NHL - Primary cutaneous CD30-positive T-cell lymphoproliferative disorder: Lymphomatoid papulosis
Specific disease: NHL - Primary cutaneous follicle center lymphoma
Specific disease: NHL - Primary cutaneous CD4-positive small or medium T-cell lymphoproliferative disorder
Specific disease: NHL - Extranodal NK / T-cell lymphoma
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 - Hyperplasia arising in immune deficiencies (e.g. PTLD)
Specific disease: NHL - Intravascular large B-cell lymphoma
Specific disease: NHL - Large B-cell lymphoma with IRF4 rearrangement
Specific disease: NHL - Mediastinal grey zone lymphoma
Specific disease: NHL - Monomorphic epitheliotropic intestinal T-cell lymphoma
Specific disease: NHL - Monomorphic PTLD (B- and T-/NK-cell types)
Specific disease: NHL - Other B-cell lymphoma
Specific disease: NHL - Other T-cell / NK-cell lymphoma
Specific disease: NHL - Polymorphic lymphoproliferative disorders arising in immune deficiency / dysregulation
Specific disease: NHL - Splenic diffuse red pulp small B-cell lymphoma
Specific disease: NHL - Indolent T-cell lymphoma of the gastrointestinal tract
Specific disease: OAL - Acute undifferentiated leukemia
Specific disease: OAL - Acute leukemia of ambiguous lineage, not otherwise specified
Specific disease: OAL - Biphenotypic leukemia
Specific disease: OAL - Mixed-phenotype acute leukemia, B/myeloid
Specific disease: OAL - Mixed phenotype acute leukemia with KMT2A rearrangement
Specific disease: OAL - Mixed-phenotype acute leukemia, T/myeloid
Specific disease: OAL - Mixed phenotype acute leukemia (MPAL) with BCR::ABL1 fusion
Specific disease: OAL - Blastic plasmacytoid dendtritic cell neoplasm
Specific disease: OND - Not otherwise specified
Specific disease: OTH_LEUK - CLL, not otherwise specified
Specific disease: OTH_LEUK - Chronic lymphocytic leukemia / small lymphocytic lymphoma
Specific disease: OTH_LEUK - Not otherwise specified
Specific disease: OTH_LEUK - Prolymphocytic Leukemia (PLL)
Specific disease: OTH_LEUK - Other leukemia, not otherwise specified
Specific disease: OTH_LEUK - T-prolymphocytic leukemia
Specific disease: PCD - Immuno-globulin-related (AL) amyloidosis
Specific disease: PCD - Monoclonal gammopathy of renal significance (MGRS)
Specific disease: PCD - Multiple myeloma
Specific disease: PCD - Multiple myeloma-IgD (heavy chain only)
Specific disease: PCD - Multiple myeloma-IgD kappa
Specific disease: PCD - Multiple myeloma-IgD lambda
Specific disease: PCD - Multiple myeloma-IgE kappa
Specific disease: PCD - Multiple myeloma-IgE lambda
Specific disease: PCD - Multiple myeloma-IgG
Specific disease: PCD - Multiple myeloma-IgG (heavy chain only)
Specific disease: PCD - Multiple myeloma-IgG kappa
Specific disease: PCD - Multiple myeloma-IgG lambda
Specific disease: PCD - Multiple myeloma-IgM (heavy chain only)
Specific disease: PCD - Multiple myeloma-IgM kappa
Specific disease: PCD - Multiple myeloma-IgM lambda
Specific disease: PCD - Multiple myeloma-Kappa (light chain only)
Specific disease: PCD - Multiple myeloma-Lambda (light chain only)
Specific disease: PCD - Multiple myeloma-IgA
Specific disease: PCD - Multiple myeloma-IgA (heavy chain only)
Specific disease: PCD - Multiple myeloma-IgA kappa
Specific disease: PCD - Multiple myeloma-IgA lambda
Specific disease: PCD - POEMS syndrome
Specific disease: PCD - Plasma cell leukemia
Specific disease: PCD - Plasmacytoma
Specific disease: PCD - Smoldering myeloma
Specific disease: PCD - Other plasma cell disorder
Specific disease: PNH - Paroxysmal nocturnal hemoglobinuria
Specific disease: RDEB - Recessive dystrophic epidermolysis bullosa
Specific disease: STU - Bone sarcoma (excluding Ewing family of tumors)
Specific disease: STU - Central nervous system tumor
Specific disease: STU - Ewing family of tumors of bone (including PNET)
Specific disease: STU - Ewing family of tumors, extraosseous (including PNET)
Specific disease: STU - Germ cell tumors, gonadal
Specific disease: STU - Germ cell tumors
Specific disease: STU - Malignant Peripheral Nerve Sheath Tumor
Specific disease: STU - Mediastinal neoplasm
Specific disease: STU - Medulloblastoma
Specific disease: STU - Not otherwise specified
Specific disease: STU - Neuroblastoma
Specific disease: STU - Ovarian (epithelial)
Specific disease: STU - Pancreatic cancer
Specific disease: STU - Renal cell carcinoma
Specific disease: STU - Retinoblastoma
Specific disease: STU - Rhabdomyosarcoma
Specific disease: STU - Testicular cancer
Specific disease: STU - Tumors of the head / neck
Specific disease: STU - Wilm's tumor
Specific disease: STU - Lung
Specific disease: STU - Other Soft tissue sarcoma (excluding Ewing family tumors)
Specific disease: STU - Synovial sarcoma
Specific disease: TIASOT - Tolerance Induction Associated With Solid Organ Transplant
Female
Male
2019 transplant year
2020 transplant year
2021 transplant year
2022 transplant year
2023 transplant year