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 Acute myeloid leukemia  
 Acute lymphoblastic leukemia (ALL) 
 Chronic myelogenous leukemia (CML) 
 Chronic lymphocytic leukemia (CLL) 
 Other leukemia  
 Myelodysplastic disorders  
 Myeloproliferative syndromes (MPS) 
 Non-Hodgkin lymphoma 
 Multiple myeloma / Plasma cell disorder 
 Solid tumors / Other malignancies 
 Severe aplastic anemia  
 Inherited abnormalities of erythrocyte differentiation or function - Hemoglobinopathy 
 Disorders of the immune system 
 Inherited disorders of metabolism  
 Histiocytic disorders 
 Inherited abnormalities of platelets 
 Autoimmune diseases and other non-malignant diseases


    1. Acute myeloid leukemia (AML or ANLL)
    2. Acute lymphoblastic leukemia (ALL)
    3. Chronic myelogenous leukemia (CML)
    4. Chronic lymphocytic leukemia (CLL)
    5. Other leukemia
      1. Acute undifferentiated leukemia
      2. Biphenotypic, bilineage or hybrid leukemia
      3. Acute mast cell leukemia
      4. Hairy cell leukemia
      5. Prolymphocytic leukemia (PLL)
       
    6. Myelodysplastic disorders
    7. Myeloproliferative syndromes (MPS)
      1. Chronic neutrophilic leukemia
      2. Chronic eosinophilic leukemia (hypereosinophilic syndrome)
      3. Polycythemia vera
      4. Chronic idiopathic myelofibrosis (with extra-medullary hematopoiesis), myelofibrosis with myeloid metaplasia, acute myelofibrosis or myelosclerosis
      5. Essential thrombocythemia
      6. Chronic MPS disorder, not otherwise specified
       
    8. Non-Hodgkin lymphoma
      1. Lymphoplasmacytic lymphoma
      2. B-cell lymphoma
      3. Follicular
      4. Mantle cell lymphoma
      5. Diffuse, large B-cell lymphomaBurkitt lymphoma / Burkitt cell leukemia
      6. Primary CNS lymphoma
      7. Mycosis fungoides
      8. Sezary syndrome
      9. T-cell lymphoma
      10. Aggressive NK-cell leukemia
      11. Waldenstrom macroglobulinemia
      12. Diffuse, small cleaved cell (Follicular center lymphoma, diffuse)
      13. Diffuse, mixed, small and large cell
      14. Diffuse, large cell
      15. Large cell, immunoblastic (B-cell only)
      16. Small noncleaved cell, unclassified
      17. Other non-Hodgkin lymphoma
       
    9. Multiple myeloma / Plasma cell disorder
      1. Multiple myeloma
      2. Plasma cell leukemia
      3. Solitary plasmacytoma (no evidence of myeloma)
      4. Primary amyloidosis
      5. Other plasma cell disorder, not otherwise specified
       
    10. Solid tumors / Other malignancies
      1. Breast cancer
      2. Lung
      3. Germ cell tumor, extragonadal
      4. Testicular
      5. Ovarian (epitheleal)
      6. Bone sarcoma, excluding Ewing family tumors
      7. Ewing family tumors of bone
      8. Fibrosarcoma
      9. Hemangiosarcoma
      10. Leiomyosarcoma
      11. Liposarcoma
      12. Lymphangio sarcoma
      13. Neurogenic sarcoma
      14. Rhabdomyosarcoma
      15. Synovial sarcoma
      16. Soft tissue sarcoma (excluding Ewing family tumors)
      17. Central nervous system tumor, including CNS PNET
      18. Medulloblastoma
      19. Neuroblastoma
      20. Head / neck
      21. Mediastinal neoplasm
      22. Colorectal
      23. Gastric
      24. Pancreatic
      25. Hepatobiliary
      26. Prostate
      27. External genitalia
      28. Cervical
      29. Uterine
      30. Vaginal
      31. Melanoma
      32. Wilm tumor
      33. Retinoblastoma
      34. Thymoma
      35. Solid tumor, not otherwise specified
      36. Renal cell
       
    11. Severe aplastic anemia
      1. Acquired amegakaryocytosis (not congenital)
      2. Acquired acquired pure red cell aplasia (not congenital)
      3. Other acquired cytopenic syndrome
      4. Paroxysmal nocturnal hemogloblinuria (PNH)
       
    12. Inherited abnormalities of erythrocyte differentiation or function - Hemoglobinopathy
      1. Shwachman-Diamond
      2. Diamond-Blackfan anemia (pure red cell aplasia)
      3. Fanconi anemia
      4. Sickle thalassemia
      5. Sickle cell disease
      6. Thalassemia, not otherwise specified
      7. Other hemoglobinopathy
       
    13. Disorders of the immune system
      1. Severe combined immunodeficiency (SCID)
      2. Absence of T and B cells SCID
      3. Absence of T, normal B cell SCID
      4. Omenn syndrome
      5. Reticular dysgenesis
      6. Bare lymphocyte syndrome
      7. Ataxia telangiectasia
      8. HIV infection
      9. DiGeorge anomaly
      10. Common variable immunodeficiency
      11. Leukocyte adhesion deficiencies
      12. Kostmann agranulocytosis (congenital neutropenia)
      13. Neutrophil actin deficiency
      14. Cartilage–hair hypoplasia
      15. CD40 ligand deficiency
      16. Other immunodeficiencies
      17. Chediak-Higashi syndrome
      18. Chronic granulomatous disease
      19. Wiskott-Aldrich syndrome
      20. X-linked lymphoproliferative syndrome
       
    14. Inherited disorders of metabolism
      1. Osteopetrosis (malignant infantile osteopetrosis)
      2. Metachromatic leukodystrophy (MLD)
      3. Adrenoleukodystrophy (ALD)
      4. Krabbe disease (Globoid leukodystrophy)
      5. Lesch-Nyhan (HGPRT deficiency)
      6. Neuronal ceroid lipofuscinosis (Batten disease)
      7. Hurler syndrome (IH)
      8. Scheie syndrome (IS)
      9. Hunter syndrome (II)
      10. Sanfilippo (III)
      11. Morquio (IV)
      12. Maroteaux-Lamy (VI)
      13. ß-glucuronidase deficiency (VII)
      14. Mucopolysaccharidosis (V)
      15. Mucopolysaccharidosis, not otherwise specified
      16. Gaucher disease
      17. Niemann-Pick disease
      18. I-cell disease
      19. Wolman disease
      20. Glucose storage disease
      21. Mucolipidoses, not otherwise specified
      22. Aspartyl glucosaminidase
      23. Fucosidosis
      24. Mannosidosis
      25. Polysaccharide hydrolase abnormality, not otherwise specified
      26. Other inherited metabolic disorder
       
    15. Histiocytic disorders
      1. Familial erythro hemophagocytic lymphohistiocytosis (FELH)
      2. Langerhans cell histiocytosis (histiocytosis-X)
      3. Hemophagocytosis (reactive or viral associated)
      4. Malignant histiocytosis
      5. Other histiocytic disorder
       
    16. Inherited abnormalities of platelets
      1. Congenital amegakaryocytosis / congenital thrombocytopenia
      2. Glanzmann thrombasthenia
      3. Other inherited platelet abnormality
       
    17. Autoimmune diseases and other non-malignant diseases
      1. Rheumatoid arthritis
      2. Psoriatic arthritis / psoriasis
      3. Juvenile idiopathic arthritis (JIA)
      4. Other arthritis
      5. Multiple sclerosis
      6. Systemic sclerosis (scleroderma)
      7. Systemic lupus erythematosus (SLE)
      8. Sjögren syndrome
      9. Polymyositis / dermatomyositis
      10. Antiphospholipid syndrome
      11. Other connective tissue disease
      12. Wegener granulomatosis
      13. Classical polyarteritis nodosa
      14. Microscopic polyarteritis nodosa
      15. Churg-strauss
      16. Giant cell arteritis
      17. Takayasu syndrome
      18. Behcet syndrome
      19. Overlap necrotizing arteritis
      20. Other vasculitis
      21. Myasthenia gravis
      22. Other autoimmune neurological disorder
      23. Idiopathic thrombocytopenic purpura (ITP)
      24. Hemolytic anemia
      25. Evan syndrome
      26. Other autoimmune cytopenia
      27. Crohn disease
      28. Ulcerative colitis
      29. Other autoimmune bowel disorder
      30. Other non-malignant diseases