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