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
Ancestral variability: American Indian or Alaska Native
Ancestral variability: Asian
Ancestral variability: Black or African American
Ancestral variability: Data unavailable
Ancestral variability: Native Hawaiian or other Pacific Islander
Ancestral variability: Multiple races
Ancestral variability: White
Cell source: Bone marrow
Cell source: Cord blood
Cell source: Peripheral blood stem cells
Cell type: HSCT
Disease category: Autoimmune disease
Disease category: Acute lymphoblastic leukemia
Disease category: Acute myeloid leukemia
Disease category: Aplastic anemia
Disease category: Chronic myeloid leukemia
Disease category: Hemoglobinopathies
Disease category: Histiocytic disease
Disease category: Hodgkin lymphoma
Disease category: Inherited bone marrow failure syndromes
Disease category: Disorders of the immune system
Disease category: Inherited disorders of metabolism
Disease category: Inherited platelet abnormalities
Disease category: Myelodysplastic diseases
Disease category: Myeloproliferative diseases
Disease category: Non-Hodgkin lymphoma
Disease category: Acute leukemia, other
Disease category: Other diseases
Disease category: Leukemia, other
Disease category: Plasma cell disease
Disease category: Paroxysmal nocturnal hemoglobinuria
Disease category: Recessive dystrophic epidermolysis bullosa
Disease category: Solid tumors
Disease category: Tolerance induction associated with solid organ transplant
Disease status: 1st remission
Disease status: 2nd or subsequent remission
Disease status: Data unavailable
Disease status: In remission
Disease status: Not applicable
Disease status: Not in remission
Donor type: Autologous
Donor type: HLA-matched sibling
Donor type: Other related donor
Donor type: Unrelated
Ancestral variability 2: Data unavailable
Ancestral variability 2: Hispanic or Latino
Ancestral variability 2: Not applicable (non-US resident)
Ancestral variability 2: Not Hispanic or Latino
Specific disease on form: Acquired amegakaryocytosis, not congenital
Specific disease on form: Acquired AA, not otherwise specified
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 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: Behçet Syndrome
Specific disease on form: Crohn's disease
Specific disease on form: Evans syndrome
Specific disease on form: Hemolytic anemia
Specific disease on form: Juvenile idiopathic arthritis, systemic, Still's disease,
Specific disease on form: Juvenile idiopathic arthritis, polyarticular
Specific disease on form: Multiple sclerosis
Specific disease on form: Myasthenia gravis
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 autoimmune disorder
Specific disease on form: Other connective tissue disease
Specific disease on form: Other vasculitis
Specific disease on form: Systemic sclerosis
Specific disease on form: B-lymphoblastic leukemia/lymphoma with BCR::ABL1 fusion
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 high hyperdiploidy
Specific disease on form: B-lymphoblastic leukemia/lymphoma with hypodiploidy
Specific disease on form: B-lymphoblastic leukemia/lymphoma, with iAMP21
Specific disease on form: B-lymphoblastic leukemia/lymphoma with IG::MYC fusion
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 PAX5alt abnormalities
Specific disease on form: B-lymphoblastic leukemia/lymphoma with TCF3::HLF fusion
Specific disease on form: B-lymphoblastic leukemia/lymphoma with TCF3::PBX1 fusion
Specific disease on form: Early T-precursor lymphoblastic leukemia/lymphoma
Specific disease on form: Natural killer, cell lymphoblastic leukemia/lymphoma
Specific disease on form: T-lymphoblastic leukemia/lymphoma
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 erythroid leukemia
Specific disease on form: Acute promyelocytic leukemia with PML::RARA fusion
Specific disease on form: Transformed to AML
Specific disease on form: Acute basophilic leukemia
Specific disease on form: Acute myeloid leukemia with BCR::ABL1 fusion
Specific disease on form: Blastic plasmacytoid dendritic cell neoplasm
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: Myeloid leukemia associated with Down syndrome
Specific disease on form: Acute myeloid leukemia with maturation
Specific disease on form: Acute myeloid leukemia with MECOM (EVI1), GATA2 rearrangement
Specific disease on form: Acute myeloid leukemia with Other MECOM rearrangements
Specific disease on form: Acute myeloid leukemia with minimal differentiation
Specific disease on form: Acute myeloid leukemia with MLLT3::KMT2A fusion
Specific disease on form: Acute myeloid leukemia with myelodysplasia, related
Specific disease on form: Myeloid sarcoma
Specific disease on form: Acute myeloid leukemia without maturation
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 with other defined genetic alterations
Specific disease on form: Acute myeloid leukemia with other KMT2A rearrangements
Specific disease on form: Acute promyelocytic leukemia with other RARA fusions
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: Therapy-related AML
Specific disease on form: Acute myeloid leukemia with mutated TP53
Specific disease on form: Ph1+; 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: Familial hemophagocytic lymphohistiocytosis, perforin deficiency, FHL2
Specific disease on form: Hemophagocytosis
Specific disease on form: Langerhans cell histiocytosis (histiocytosis-X)
Specific disease on form: Malignant histiocytosis
Specific disease on form: Familial hemophagocytic lymphohistiocytosis, no mutation identified
Specific disease on form: Histiocytic disorder, not otherwise specified
Specific disease on form: Other histiocytic disorder
Specific disease on form: Familial hemophagocytic lymphohistiocytosis, other mutations
Specific disease on form: Familial hemophagocytic lymphohistiocytosis, STXBP2, FHL5
Specific disease on form: Familial hemophagocytic lymphohistiocytosis, UNC13D, FHL3
Specific disease on form: Classic Hodgkin lymphoma
Specific disease on form: Lymphocyte-depleted
Specific disease on form: Lymphocyte-rich
Specific disease on form: Mixed cellularity
Specific disease on form: Nodular lymphocyte predominant Hodgkin lymphoma
Specific disease on form: Nodular sclerosis
Specific disease on form: Hodgkin lymphoma, not otherwise specified
Specific disease on form: Diamond-Blackfan anemia
Specific disease on form: Telomere biology disorders, including dyskeratosis congenita (DKC1, TERT, TERC, and other mutations)
Specific disease on form: Fanconi anemia
Specific disease on form: Other inherited bone marrow failure syndrome
Specific disease on form: Germline SAMD9 variant, MIRAGE syndrome
Specific disease on form: Severe congenital neutropenia
Specific disease on form: Shwachman-Diamond
Specific disease on form: Wolman disease
Specific disease on form: Other constitutional anemia
Specific disease on form: Ataxia telangiectasia
Specific disease on form: Autoimmune lymphoproliferative syndrome
Specific disease on form: Bare lymphocyte syndrome
Specific disease on form: Cartilage-hair hypoplasia
Specific disease on form: CD40 ligand deficiency
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: CTLA4 deficiency
Specific disease on form: DiGeorge anomaly
Specific disease on form: DOCK8 deficiency
Specific disease on form: GATA2 deficiency
Specific disease on form: Griscelli syndrome type 2
Specific disease on form: Immune deficiency, not otherwise specified
Specific disease on form: Immune dysregulation polyendocrinopathy, enteropathy X-linked, FOXP3 deficiency
Specific disease on form: Leukocyte adhesion deficiencies
Specific disease on form: LRBA deficiency
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: Absence of T and B-cells SCID
Specific disease on form: Absence of T, normal B-cell SCID
Specific disease on form: SCID, T- B- NK-, adenosine deaminase (ADA) deficiency
Specific disease on form: SCID,T- B+ NK+, ILR alpha deficiency
Specific disease on form: SCID, T- B- NK+, DCLRE1C (Artemis) deficiency
Specific disease on form: SCID, T- B+ NK-, IL2RG mutations, X-linked SCID
Specific disease on form: SCID, not otherwise specified
Specific disease on form: SCID, T- B- NK+, RAG 1/2 deficiency
Specific disease on form: SCID, T- B- NK-, reticular dysgenesis
Specific disease on form: SCID, T- B- NK-, not otherwise specified
Specific disease on form: STAT1 gain of function
Specific disease on form: STAT3 gain of function
Specific disease on form: Wiskott-Aldrich syndrome
Specific disease on form: XIAP-2 Deficiency
Specific disease on form: Adrenoleukodystrophy
Specific disease on form: Beta-glucuronidase deficiency VII
Specific disease on form: Fucosidosis
Specific disease on form: Hereditary diffuse leukoencephalopathy with spheroids
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: Mannosidosis
Specific disease on form: Maroteaux-lamy VI
Specific disease on form: Metachromatic leukodystrophy
Specific disease on form: Morquio syndrome, MPS-IV
Specific disease on form: Mucopolysaccharidosis, not otherwise specified
Specific disease on form: Neuronal ceroid lipofuscinosis, Batten disease
Specific disease on form: Inherited metabolic disorder, not otherwise specified
Specific disease on form: Osteopetrosis (malignant infantile osteopetrosis)
Specific disease on form: Other inherited metabolic disorder
Specific disease on form: Sanfilippo syndrome, MPS-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: Myelodysplastic syndrome with biallelic TP53 inactivation
Specific disease on form: Refractory cytopenia of childhood
Specific disease on form: Childhood MDS with increased blasts
Specific disease on form: Childhood MDS with low blasts, hypocellular
Specific disease on form: Childhood MDS with low blasts, not otherwise specified
Specific disease on form: Chronic myelomonocytic leukemia, myelodysplastic
Specific disease on form: Chronic myelomonocytic leukemia, myeloproliferative
Specific disease on form: Myelodysplastic syndrome with increased blasts
Specific disease on form: Myelodysplastic syndrome with fibrosis
Specific disease on form: Myelodysplastic syndrome, hypoplastic (MDS-h) <=25% cellularity by age
Specific disease on form: Juvenile myelomonocytic leukemia
Specific disease on form: Myelodysplastic syndrome with low blasts and ring sideroblasts
Specific disease on form: Mastocytosis
Specific disease on form: Chronic myelomonocytic leukemia
Specific disease on form: Myelodysplastic/myeloproliferative neoplasm with neutrophilia
Specific disease on form: Myelodysplastic syndrome/myeloproliferative neoplasm, not otherwise specified
Specific disease on form: MDS/MPN with ring sideroblasts and thrombocytosis
Specific disease on form: MDS/MPN with ring sideroblasts. >=15% ring sideroblasts and wild type SF3B1, and thrombocytosis
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: RARS
Specific disease on form: MDS-RS with multilineage dysplasia
Specific disease on form: MDS-RS with single lineage dysplasia
Specific disease on form: Myelodysplastic syndrome with low blasts and SF3B1 mutation (MDS-SF3B1)
Specific disease on form: Myelodysplastic/myeloproliferative neoplasm with SF3B1 mutation and thrombocytosis
Specific disease on form: Myelodysplastic/myeloproliferative neoplasm with SF3B1 mutation and thrombocytosis (MDS/MPN–RS–T)
Specific disease on form: Myelodysplastic syndrome with single lineage dysplasia
Specific disease on form: MDS unclassifiable, not otherwise specified
Specific disease on form: Myelodysplastic syndrome with low blasts, MDS-LB; <5% BM, <2% PBSC
Specific disease on form: Myelodysplastic syndrome with low blasts and isolated 5q deletion
Specific disease on form: Multiple myeloma, light chain only
Specific disease on form: Multiple myeloma, multiple chain
Specific disease on form: Multiple myeloma, non-secretory
Specific disease on form: Smoldering myeloma
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
Specific disease on form: Myeloid/lymphoid neoplasms with PDGFRA rearrangement
Specific disease on form: Primary myelofibrosis
Specific disease on form: Polycythemia vera (PCV)
Specific disease on form: Post-essential thrombocythemic myelofibrosis
Specific disease on form: Post-polycythemic myelofibrosis
Specific disease on form: Systemic mastocytosis
Specific disease on form: Myeloproliferative neoplasm, unclassifiable
Specific disease on form: Adult T-cell lymphoma/leukemia
Specific disease on form: Aggressive NK-cell leukemia
Specific disease on form: ALK-negative anaplastic large-cell lymphoma
Specific disease on form: ALK-positive anaplastic large-cell lymphoma
Specific disease on form: Breast implant-associated anaplastic large-cell lymphoma
Specific disease on form: Burkitt lymphoma
Specific disease on form: Primary cutaneous CD30-positive T-cell lymphoproliferative disorder: Primary cutaneous anaplastic large cell lymphoma
Specific disease on form: Classical Hodgkin lymphoma PTLD
Specific disease on form: Primary cutaneous CD30-positive T-cell lymphoproliferative disorder, lymphomatoid papulosis
Specific disease on form: Primary cutaneous CD4-positive small or medium T-cell lymphoproliferative disorder
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 cutaneous follicle center lymphoma
Specific disease on form: Primary cutaneous gamma/delta T-cell lymphoma
Specific disease on form: Primary large B-cell lymphoma of the CNS
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, germinal center B-cell subtype
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, BCL2, and BCL6 rearrangements
Specific disease on form: Diffuse large B-cell lymphoma/high-grade B-cell lymphoma with MYC and BCL6 rearrangements
Specific disease on form: Diffuse large B-cell lymphoma, not otherwise specified
Specific disease on form: EBV-positive diffuse large B-cell lymphoma
Specific disease on form: EBV-positive nodal T- and NK-cell lymphoma
Specific disease on form: Enteropathy-associated T-cell lymphoma
Specific disease on form: Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT)
Specific disease on form: Extranodal NKT-cell lymphoma
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 with 11q aberration
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, not otherwise specified
Specific disease on form: Hyperplasia arising in immune deficiencies (e.g., PTLD)
Specific disease on form: IgM-LPL/Waldenstrom macroglobulinemia
Specific disease on form: Intestinal T-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: NK-large granular lymphocytic leukemia
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: Mediastinal grey zone lymphoma
Specific disease on form: Monomorphic epitheliotropic intestinal T-cell lymphoma
Specific disease on form: Monomorphic PTLD (B-, T-, or NK-cell types)
Specific disease on form: Mycosis fungoides
Specific disease on form: Nodal marginal zone lymphoma
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 TFH cell lymphoma, not otherwise specified
Specific disease on form: Other B-cell lymphoma
Specific disease on form: Other T-cell/NK-cell lymphoma
Specific disease on form: Primary cutaneous CD30+ T-cell lymphoproliferative disorders [Primary cutaneous anaplastic large-cell lymphoma (C-ALCL), lymphoid papulosis]
Specific disease on form: Primary large B-cell lymphoma of the vitreoretina
Specific disease on form: Primary cutaneous peripheral T-cell lymphoma, not otherwise specified
Specific disease on form: Plasmablastic lymphoma
Specific disease on form: Polymorphic lymphoproliferative disorders arising in immune deficiency/dysregulation
Specific disease on form: Primary effusion lymphoma
Specific disease on form: Primary mediastinal large B-cell lymphoma
Specific disease on form: Peripheral T-cell lymphoma, not otherwise specified
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-positive T-cell lymphoma of childhood
Specific disease on form: T-cell/histiocytic-rich large B-cell lymphoma
Specific disease on form: Transformations of indolent B-cell lymphomas
Specific disease on form: Waldenströom macroglobulinemia/lymphoplasmacytic lymphoma
Specific disease on form: Acute leukemia of ambiguous lineage, not otherwise specified
Specific disease on form: Acute undifferentiated leukemia
Specific disease on form: Mixed phenotype acute leukemia with BCR::ABL1 fusion
Specific disease on form: Mixed phenotype acute leukemia, B/myeloid
Specific disease on form: Mixed phenotype acute leukemia, T/myeloid
Specific disease on form: Mixed phenotype acute leukemia, rare types
Specific disease on form: Mixed phenotype acute leukemia with KMT2A rearrangement
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: Other leukemia, not otherwise specified
Specific disease on form: Other plasma cell disorder
Specific disease on form: PLL, B-cell
Specific disease on form: Prolymphocytic leukemia (PLL), not otherwise specified
Specific disease on form: T-prolymphocytic leukemia
Specific disease on form: Immunoglobulin-related amyloidosis
Specific disease on form: Monoclonal gammopathy of renal significance
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: 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: Plasma cell leukemia
Specific disease on form: Plasmacytoma
Specific disease on form: POEMS syndrome
Specific disease on form: Paroxysmal nocturnal hemoglobinuria
Specific disease on form: Recessive dystrophic epidermolysis bullosa
Specific disease on form: Lung, not otherwise specified
Specific disease on form: Bone sarcoma, excluding Ewing family of tumors
Specific disease on form: Central nervous system tumor, including CNS PNET
Specific disease on form: Ewing family of tumors of bone, including peripheral neural ectodermal tumor
Specific disease on form: Ewing family of tumors, extraosseous, including peripheral neural ectodermal tumor
Specific disease on form: Germ cell tumor, extragonadal
Specific disease on form: Germ cell tumors, gonadal
Specific disease on form: Glioblastoma multiforme
Specific disease on form: Malignant rhabdoid tumor of the kidney
Specific disease on form: Mediastinal neoplasm
Specific disease on form: Medulloblastoma
Specific disease on form: Malignant peripheral nerve sheath tumor
Specific disease on form: Neuroblastoma
Specific disease on form: Solid tumor, not otherwise specified
Specific disease on form: Other solid tumor
Specific disease on form: Other soft tissue sarcoma, excluding Ewing family of tumors
Specific disease on form: Ovarian, epithelial
Specific disease on form: Pancreatic
Specific disease on form: Renal cell
Specific disease on form: Retinoblastoma
Specific disease on form: Rhabdomyosarcoma
Specific disease on form: Synovial sarcoma
Specific disease on form: Atypical teratoid rhabdoid tumor
Specific disease on form: Testicular
Specific disease on form: Tumors of the head/neck
Specific disease on form: Wilms tumor
Specific disease on form: Chronic myeloid leukemia - Unknown
Specific disease on form: Other diseases - Unknown
Specific disease on form: Tolerance induction associated with solid organ transplant - Unknown
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: AA - Acquired AA, secondary to hepatitis
Specific disease: Autoimmune disease - Crohn's disease
Specific disease: Autoimmune disease - Evans syndrome
Specific disease: Autoimmune disease - Hemolytic anemia
Specific disease: Autoimmune disease - Juvenile idiopathic arthritis, polyarticular
Specific disease: Autoimmune disease - Juvenile idiopathic arthritis, systemic, Still's disease,
Specific disease: Autoimmune disease - Multiple sclerosis
Specific disease: Autoimmune disease - Myasthenia gravis
Specific disease: Autoimmune disease - Other autoimmune neurologic disease
Specific disease: Autoimmune disease - Other connective tissue disease
Specific disease: Autoimmune disease - Other autoimmune bowel disease
Specific disease: Autoimmune disease - Other autoimmune cytopenia, low blood counts
Specific disease: Autoimmune disease - Other autoimmune disease
Specific disease: Autoimmune disease - Other vasculitis
Specific disease: Autoimmune disease - Systemic sclerosis
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 high hyperdiploidy
Specific disease: ALL - B-lymphoblastic leukemia/lymphoma with hypodiploidy
Specific disease: ALL - B-lymphoblastic leukemia/lymphoma, with iAMP21
Specific disease: ALL - B-lymphoblastic leukemia/lymphoma with IG::MYC 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 PAX5alt abnormalities
Specific disease: ALL - B-lymphoblastic leukemia/lymphoma with TCF3::HLF fusion
Specific disease: ALL - B-lymphoblastic leukemia/lymphoma with TCF3::PBX1 fusion
Specific disease: ALL - Early T-precursor lymphoblastic leukemia/lymphoma
Specific disease: ALL - Natural killer, cell lymphoblastic leukemia/lymphoma
Specific disease: ALL - T-lymphoblastic leukemia/lymphoma
Specific disease: AML_ANLL - Acute basophilic leukemia
Specific disease: AML_ANLL - Acute erythroid leukemia
Specific disease: AML_ANLL - Acute megakaryoblastic leukemia
Specific disease: AML_ANLL - Acute monocytic leukemia
Specific disease: AML_ANLL - Acute myelomonocytic leukemia
Specific disease: AML_ANLL - Acute promyelocytic leukemia with other RARA fusions
Specific disease: AML_ANLL - Acute promyelocytic leukemia with PML::RARA fusion
Specific disease: AML_ANLL - Transformed to AML
Specific disease: AML_ANLL - Acute myeloid leukemia with BCR::ABL1 fusion
Specific disease: AML_ANLL - Acute myeloid leukemia with CBFB::MYH11 fusion
Specific disease: AML_ANLL - Acute myeloid leukemia with CEBPA mutation
Specific disease: AML_ANLL - Acute myeloid leukemia with DEK::NUP214 fusion
Specific disease: AML_ANLL - Myeloid leukemia associated with Down syndrome
Specific disease: AML_ANLL - Acute myeloid leukemia with MECOM (EVI1), GATA2 rearrangement
Specific disease: AML_ANLL - Acute myeloid leukemia with maturation
Specific disease: AML_ANLL - Acute panmyelosis with myelofibrosis
Specific disease: AML_ANLL - Acute myeloid leukemia with minimal differentiation
Specific disease: AML_ANLL - Acute myeloid leukemia with MLLT3::KMT2A fusion
Specific disease: AML_ANLL - Acute myeloid leukemia with myelodysplasia, related
Specific disease: AML_ANLL - Myeloid sarcoma
Specific disease: AML_ANLL - Acute myeloid leukemia with NPM1 mutation
Specific disease: AML_ANLL - Acute myeloid leukemia without maturation
Specific disease: AML_ANLL - Acute myeloid leukemia, not otherwise specified
Specific disease: AML_ANLL - Acute myeloid leukemia with NUP98 rearrangement
Specific disease: AML_ANLL - Acute myeloid leukemia with other defined genetic alterations
Specific disease: AML_ANLL - Acute myeloid leukemia with other KMT2A rearrangements
Specific disease: AML_ANLL - Acute myeloid leukemia with Other MECOM rearrangements
Specific disease: AML_ANLL - Acute myeloid leukemia with RBM15::MRTFA fusion
Specific disease: AML_ANLL - AML with mutated RUNX1, provisional entity
Specific disease: AML_ANLL - Acute myeloid leukemia with RUNX1::RUNX1T1 fusion
Specific disease: AML_ANLL - Therapy-related AML
Specific disease: AML_ANLL - Acute myeloid leukemia with mutated TP53
Specific disease: Autoimmune disease - Behçet syndrome
Specific disease: CML - Chronic myeloid leukemia
Specific disease: Hemoglobinopathies - Other hemoglobinopathy
Specific disease: Hemoglobinopathies - Sickle cell anemia
Specific disease: Hemoglobinopathies - Transfusion-dependent thalassemia
Specific disease: Histiocytic disease - Familial hemophagocytic lymphohistiocytosis, perforin deficiency, FHL2
Specific disease: Histiocytic disease - Familial hemophagocytic lymphohistiocytosis, UNC13D, FHL3
Specific disease: Histiocytic disease - Familial hemophagocytic lymphohistiocytosis, STXBP2, FHL5
Specific disease: Histiocytic disease - Familial hemophagocytic lymphohistiocytosis, no mutation identified
Specific disease: Histiocytic disease - Familial hemophagocytic lymphohistiocytosis, other mutations
Specific disease: Histiocytic disease - Hemophagocytic lymphohistiocytosis
Specific disease: Histiocytic disease - Hemophagocytosis
Specific disease: Histiocytic disease - Langerhans cell histiocytosis
Specific disease: Histiocytic disease - Malignant histiocytosis
Specific disease: Histiocytic disease - Not otherwise specified
Specific disease: Histiocytic disease - Other histiocytic disease
Specific disease: HL - Classic Hodgkin lymphoma
Specific disease: HL - Classical Hodgkin lymphoma PTLD
Specific disease: HL - Hodgkin lymphoma, not otherwise specified
Specific disease: HL - Lymphocyte-depleted
Specific disease: HL - Lymphocyte-rich
Specific disease: HL - Mixed cellularity
Specific disease: HL - Nodular lymphocyte predominant
Specific disease: HL - Nodular sclerosis
Specific disease: Inherited disorders of metabolism - Beta-glucuronidase deficiency VII
Specific disease: Inherited bone marrow failure syndromes - Diamond-Blackfan anemia
Specific disease: Inherited bone marrow failure syndromes - Telomere biology disorders, including dyskeratosis congenita (DKC1, TERT, TERC, and other mutations)
Specific disease: Inherited bone marrow failure syndromes - Fanconi anemia
Specific disease: Inherited bone marrow failure syndromes - Germline SAMD9 variant, MIRAGE syndrome
Specific disease: Inherited bone marrow failure syndromes - Other constitutional anemia
Specific disease: Inherited bone marrow failure syndromes - Other inherited bone marrow failure syndrome
Specific disease: Inherited bone marrow failure syndromes - Severe congenital neutropenia
Specific disease: Inherited bone marrow failure syndromes - Shwachman-Diamond syndrome
Specific disease: Disorders of the immune system - Autoimmune lymphoproliferative syndrome
Specific disease: Disorders of the immune system - Ataxia telangiectasia
Specific disease: Disorders of the immune system - Bare lymphocyte syndrome
Specific disease: Disorders of the immune system - Cartilage-hair hypoplasia
Specific disease: Disorders of the immune system - CD40 ligand deficiency
Specific disease: Disorders of the immune system - Chediak-Higashi syndrome
Specific disease: Disorders of the immune system - Chronic granulomatous disease
Specific disease: Disorders of the immune system - Common variable immunodeficiency
Specific disease: Disorders of the immune system - CTLA4 deficiency
Specific disease: Disorders of the immune system - DiGeorge anomaly
Specific disease: Disorders of the immune system - DOCK8 deficiency
Specific disease: Disorders of the immune system - GATA2 deficiency
Specific disease: Disorders of the immune system - Griscelli syndrome type 2
Specific disease: Disorders of the immune system - Immune deficiency
Specific disease: Disorders of the immune system - Immune dysregulation polyendocrinopathy, enteropathy X-linked, FOXP3 deficiency
Specific disease: Disorders of the immune system - Leukocyte adhesion deficiencies
Specific disease: Disorders of the immune system - LRBA deficiency
Specific disease: Disorders of the immune system - MHC class II deficiency, bare lymphocyte syndrome
Specific disease: Disorders of the immune system - NEMO deficiency syndrome
Specific disease: Disorders of the immune system - Not otherwise specified
Specific disease: Disorders of the immune system - Omenn syndrome
Specific disease: Disorders of the immune system - SAP deficiency, XIAP-1
Specific disease: Disorders of the immune system - Severe combined immunodeficiency (SCID)
Specific disease: Disorders of the immune system - SCID, T- B- NK-, adenosine deaminase (ADA) deficiency
Specific disease: Disorders of the immune system - SCID,T- B+ NK+, ILR alpha deficiency
Specific disease: Disorders of the immune system - SCID, T- B- NK+, DCLRE1C (Artemis) deficiency
Specific disease: Disorders of the immune system - SCID, T- B+ NK-, IL2RG mutations, X-linked SCID
Specific disease: Disorders of the immune system - SCID, T- B- NK+, RAG 1/2 deficiency
Specific disease: Disorders of the immune system - SCID, T- B- NK-, reticular dysgenesis
Specific disease: Disorders of the immune system - SCID, T- B- NK-, not otherwise specified
Specific disease: Disorders of the immune system - STAT1 gain of function
Specific disease: Disorders of the immune system - STAT3 gain of function
Specific disease: Disorders of the immune system - Absence of T, normal B-cell SCID
Specific disease: Disorders of the immune system - Wiskott-Aldrich syndrome
Specific disease: Disorders of the immune system - XIAP-2 Deficiency
Specific disease: Inherited disorders of metabolism - Adrenoleukodystrophy
Specific disease: Inherited disorders of metabolism - Fucosidosis
Specific disease: Inherited disorders of metabolism - Hereditary diffuse leukoencephalopathy with spheroids
Specific disease: Inherited disorders of metabolism - Hunter syndrome
Specific disease: Inherited disorders of metabolism - Hurler syndrome, MPS-IH or MPS I
Specific disease: Inherited disorders of metabolism - Krabbe disease
Specific disease: Inherited disorders of metabolism - Mannosidosis
Specific disease: Inherited disorders of metabolism - Maroteaux-lamy
Specific disease: Inherited disorders of metabolism - Metachromatic leukodystrophy
Specific disease: Inherited disorders of metabolism - Morquio syndrome, MPS-IV
Specific disease: Inherited disorders of metabolism - Mucopolysaccharidosis, not otherwise specified
Specific disease: Inherited disorders of metabolism - Neuronal ceroid lipofuscinosis, Batten disease
Specific disease: Inherited disorders of metabolism - Not otherwise specified
Specific disease: Inherited disorders of metabolism - Osteopetrosis
Specific disease: Inherited disorders of metabolism - Sanfilippo syndrome, MPS-III
Specific disease: Inherited disorders of metabolism - Wolman disease
Specific disease: Inherited platelet abnormalities - Congenital amegakaryocytosis/congenital thrombocytopenia
Specific disease: Inherited platelet abnormalities - Glanzmann thrombasthenia
Specific disease: Inherited platelet abnormalities - Other inherited platelet abnormality
Specific disease: MDS - Myelodysplastic syndrome with biallelic TP53 inactivation
Specific disease: MDS - Childhood MDS with increased blasts
Specific disease: MDS - Childhood MDS with low blasts, not otherwise specified
Specific disease: MDS - Childhood MDS with low blasts, hypocellular
Specific disease: MDS - Chronic myelomonocytic leukemia, myelodysplastic
Specific disease: MDS - Chronic myelomonocytic leukemia, myeloproliferative
Specific disease: MDS - Myelodysplastic syndrome with fibrosis
Specific disease: MDS - Myelodysplastic syndrome, hypoplastic (MDS-h) <=25% cellularity by age
Specific disease: MDS - Myelodysplastic syndrome with increased blasts
Specific disease: MDS - Juvenile myelomonocytic leukemia
Specific disease: MDS - Myelodysplastic syndrome with low blasts and ring sideroblasts
Specific disease: MPN - Mastocytosis
Specific disease: MDS - Chronic myelomonocytic leukemia
Specific disease: MDS - Myelodysplastic/myeloproliferative neoplasm with neutrophilia
Specific disease: MDS - Myelodysplastic syndrome/myeloproliferative neoplasm, not otherwise specified
Specific disease: MDS - MDS/MPN with ring sideroblasts and thrombocytosis
Specific disease: MDS - MDS/MPN with ring sideroblasts. >=15% ring sideroblasts and wild type SF3B1, and thrombocytosis
Specific disease: MDS - Myelodysplastic syndrome with multilineage dysplasia
Specific disease: MDS - Not otherwise specified
Specific disease: MDS - Refractory anemia with ringed sideroblasts
Specific disease: MDS - Refractory cytopenia of childhood
Specific disease: MDS - MDS-RS with multilineage dysplasia
Specific disease: MDS - MDS-RS with single lineage dysplasia
Specific disease: MDS - Myelodysplastic syndrome with low blasts and SF3B1 mutation (MDS-SF3B1)
Specific disease: MDS - Myelodysplastic/myeloproliferative neoplasm with SF3B1 mutation and thrombocytosis
Specific disease: MDS - Myelodysplastic syndrome with single lineage dysplasia
Specific disease: MDS - Myelodysplastic syndrome with low blasts, MDS-LB; <5% BM, <2% PBSC
Specific disease: MDS - Myelodysplastic syndrome with low blasts and isolated 5q deletion
Specific disease: PCD - 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
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 - Polycythemia vera (PCV)
Specific disease: MPN - Post-essential thrombocythemic myelofibrosis
Specific disease: MPN - Post-polycythemic myelofibrosis
Specific disease: MPN - Primary myelofibrosis
Specific disease: MPN - Myeloproliferative neoplasm, unclassifiable
Specific disease: NHL - Adult T-cell lymphoma/leukemia
Specific disease: NHL - Aggressive NK-cell leukemia
Specific disease: NHL - ALK-negative anaplastic large-cell lymphoma
Specific disease: NHL - ALK-positive anaplastic large-cell lymphoma
Specific disease: NHL - Breast implant-associated anaplastic large-cell lymphoma
Specific disease: NHL - High-grade B-cell lymphoma with 11q aberration
Specific disease: NHL - Burkitt lymphoma
Specific disease: NHL - Primary cutaneous CD30-positive T-cell lymphoproliferative disorder: Primary cutaneous anaplastic large cell lymphoma
Specific disease: NHL - Primary cutaneous CD30-positive T-cell lymphoproliferative disorder, lymphomatoid papulosis
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 cutaneous follicle center lymphoma
Specific disease: NHL - Primary cutaneous gamma/delta T-cell lymphoma
Specific disease: NHL - Primary large B-cell lymphoma of the CNS
Specific disease: NHL - Primary cutaneous CD4-positive small or medium T-cell lymphoproliferative disorder
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, germinal center B-cell subtype
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, BCL2, and BCL6 rearrangements
Specific disease: NHL - Diffuse large B-cell lymphoma/high-grade B-cell lymphoma with MYC and BCL6 rearrangements
Specific disease: NHL - Diffuse large B-cell lymphoma, not otherwise specified
Specific disease: NHL - EBV-positive diffuse large B-cell lymphoma
Specific disease: NHL - EBV-positive nodal T- and NK-cell lymphoma
Specific disease: NHL - Enteropathy-associated T-cell lymphoma
Specific disease: NHL - Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT)
Specific disease: NHL - Extranodal NKT-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 - Hepatosplenic T-cell lymphoma
Specific disease: NHL - High-grade B-cell lymphoma, with MYC and BCL2 and/or BCL6 rearrangements
Specific disease: NHL - High-grade B-cell lymphoma, not otherwise specified
Specific disease: NHL - Hyperplasia arising in immune deficiencies (e.g., PTLD)
Specific disease: NHL - Intestinal T-cell lymphoma, not otherwise specified
Specific disease: NHL - Intravascular large B-cell lymphoma
Specific disease: NHL - KSHV/HHV8-positive diffuse large B-cell lymphoma
Specific disease: NHL - ALK-positive large B-cell lymphoma
Specific disease: NHL - Large B-cell lymphoma with IRF4 rearrangement
Specific disease: NHL - NK-large granular lymphocytic leukemia
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 - Mediastinal grey zone lymphoma
Specific disease: NHL - Monomorphic epitheliotropic intestinal T-cell lymphoma
Specific disease: NHL - Monomorphic PTLD (B-, T-, or NK-cell types)
Specific disease: NHL - Mycosis fungoides
Specific disease: NHL - Nodal marginal zone lymphoma
Specific disease: NHL - Nodal TFH cell lymphoma, angioimmunoblastic-type
Specific disease: NHL - Nodal TFH cell lymphoma, follicular-type
Specific disease: NHL - Nodal TFH cell lymphoma, not otherwise specified
Specific disease: NHL - Other B-cell lymphoma
Specific disease: NHL - Other T-cell/NK-cell lymphoma
Specific disease: NHL - Primary cutaneous CD30+ T-cell lymphoproliferative disorders [Primary cutaneous anaplastic large-cell lymphoma (C-ALCL), lymphoid papulosis]
Specific disease: NHL - Primary large B-cell lymphoma of the vitreoretina
Specific disease: NHL - Primary cutaneous peripheral T-cell lymphoma, not otherwise specified
Specific disease: NHL - Peripheral T-cell lymphoma, not otherwise specified
Specific disease: NHL - Plasmablastic lymphoma
Specific disease: NHL - Polymorphic lymphoproliferative disorders arising in immune deficiency/dysregulation
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-positive T-cell lymphoma of childhood
Specific disease: NHL - Primary mediastinal large B-cell lymphoma
Specific disease: NHL - Transformations of indolent B-cell lymphomas
Specific disease: NHL - IgM-LPL/Waldenstrom macroglobulinemia
Specific disease: NHL - Waldenströom macroglobulinemia/lymphoplasmacytic lymphoma
Specific disease: Acute leukemia, other - Acute leukemia of ambiguous lineage, not otherwise specified
Specific disease: Acute leukemia, other - Acute undifferentiated leukemia
Specific disease: Acute leukemia, other - Blastic plasmacytoid dendritic cell neoplasm
Specific disease: Acute leukemia, other - Mixed phenotype acute leukemia with BCR::ABL1 fusion
Specific disease: Acute leukemia, other - Mixed phenotype acute leukemia, B/myeloid
Specific disease: Acute leukemia, other - Mixed phenotype acute leukemia, T/myeloid
Specific disease: Acute leukemia, other - Mixed phenotype acute leukemia, rare types
Specific disease: Acute leukemia, other - Mixed phenotype acute leukemia with KMT2A rearrangement
Specific disease: Other disease - Not otherwise specified
Specific disease: Other leukemia - CLL, not otherwise specified
Specific disease: Other leukemia - Chronic lymphocytic leukemia/small lymphocytic lymphoma
Specific disease: Other leukemia - Hairy cell leukemia
Specific disease: Other leukemia - Not otherwise specified
Specific disease: Other leukemia - Prolymphocytic leukemia (PLL)
Specific disease: Other leukemia - Prolymphocytic leukemia
Specific disease: Other leukemia - T-prolymphocytic leukemia
Specific disease: PCD - Immunoglobulin-related amyloidosis
Specific disease: PCD - Monoclonal gammopathy of renal significance
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, 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, heavy chain only
Specific disease: PCD - Multiple myeloma, IgA kappa
Specific disease: PCD - Multiple myeloma, IgA lambda
Specific disease: PCD - Other plasma cell disorder
Specific disease: PCD - Plasma cell leukemia
Specific disease: PCD - Plasmacytoma
Specific disease: PCD - POEMS syndrome
Specific disease: PCD - Smoldering myeloma
Specific disease: PNH - Paroxysmal nocturnal hemoglobinuria
Specific disease: RDEB - Recessive dystrophic epidermolysis bullosa
Specific disease: Solid tumors - Atypical teratoid rhabdoid tumor
Specific disease: Solid tumors - Bone sarcoma, excluding Ewing family of tumors
Specific disease: Solid tumors - Central nervous system tumor
Specific disease: Solid tumors - Ewing family of tumors of bone, including peripheral neural ectodermal tumor
Specific disease: Solid tumors - Ewing family of tumors, extraosseous, including peripheral neural ectodermal tumor
Specific disease: Solid tumors - Glioblastoma multiforme
Specific disease: Solid tumors - Germ cell tumors, gonadal
Specific disease: Solid tumors - Germ cell tumors
Specific disease: Solid tumors - Lung
Specific disease: Solid tumors - Malignant rhabdoid tumor of the kidney
Specific disease: Solid tumors - Mediastinal neoplasm
Specific disease: Solid tumors - Medulloblastoma
Specific disease: Solid tumors - Malignant peripheral nerve sheath tumor
Specific disease: Solid tumors - Neuroblastoma
Specific disease: Solid tumors - Not otherwise specified
Specific disease: Solid tumors - Other soft tissue sarcoma, excluding Ewing family of tumors
Specific disease: Solid tumors - Ovarian, epithelial
Specific disease: Solid tumors - Pancreatic
Specific disease: Solid tumors - Renal cell carcinoma
Specific disease: Solid tumors - Retinoblastoma
Specific disease: Solid tumors - Rhabdomyosarcoma
Specific disease: Solid tumors - Synovial sarcoma
Specific disease: Solid tumors - Testicular
Specific disease: Solid tumors - Tumors of the head/neck
Specific disease: Solid tumors - Wilms tumor
Specific disease: Tolerance induction associated with solid organ transplant
Sex: Female
Sex: Male
Transplant year: 2020
Transplant year: 2021
Transplant year: 2022
Transplant year: 2023
Transplant year: 2024