AML AML AML AML AML ALL AML MPN AML
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1 Absence of T & B cells SCID Absence of T, normal B cell SCID Acquired cytopenic syndrome Acquired immune deficiency syndrome (HIV infection) Acquired Pure Red Cell Aplasia (PRCA) Acute undifferentiated leukaemia Acute biphenotypic leukaemia Acute leukaemia, secondary to previous MDS diagnosis Acute leukaemia, secondary to previous diagnosis Acute leukaemia, secondary to treatment of primary disease Acute lymphocytic leukaemia Acute mast cell leukaemia Acute myelofibrosis (Chronic idiopathic myelofibrosis) Acute myeloid leukaemia Acute myelosclerosis (Chronic idiopathic myelofibrosis) ADA deficiency (SCID) Adenocarcinoma origin X Adenosine deaminase deficiency (SCID) (ADA) Adrenoleukodystrophy Adult T-cell lymphoma/leukaemia (HTLV1+) Aggressive NK-cell leukaemia Agranulocytosis (Kostmann) AIDS (HIV infection) AILD (Angioimmunoblastic lymphoma T-cell) Albers-Schonberg Disease (Osteopetrosis) ALS (Amyotrophic lateral sclerosis) Amegakaryocytosis acquired Amegakaryocytosis (congenital) Amyloidosis Amyotrophic lateral sclerosis Anaplastic large-cell, T/null cell types Anaplastic large-cell, T/null cell, primary cutaneous lymphoma Anaplastic large-cell, T/null cell, primary systemic lymphoma Angioimmunoblastic lymphoma T-cell (AILD) Angiosarcoma Antiphospholipid syndrome Aplastic anaemia Aspartyl glucosaminuria Astrocytoma Ataxia telangiectasia Atypic Hairy Cell Leukaemia Atypical s Autoimmune lymphoproliferative syndrome Bare lymphocyte/lack of HLA- antig xp Batten disease (Neuronal ceriod lipofuscinosis) B-Cell Lymphocytic Leukaemia B-cell lymphomas (NHL), unspecified Behçet s syndrome Berlin breakage syndrome B-glucuronidase deficiency (VII) Blast NK cell Blastic Plasmacytoid Dendritic Cell Neoplasm (BPDCN) Bone sarcoma (exclude Ewing sarcoma, include PNET sarcoma) BM failure-saa BM failure-saa BM failure-other BM failure-saa Lymphoblastic Lymphoma
2 BPDCN Breast Cancer (Inflammatory / Non inflammatory) Burkitt cell leukemia Burkitt s lymphoma Cartilage hair hypoplasia Castleman's disease Diagnosis CD40 ligand deficiency Central nervous system (include CNS PNET) Chediak-Higashi syndrome Choriocarcinoma Chronic eosinophylic leukaemia Chronic granulomatous disease Chronic inflammatory demyelinating polyneuropathy Chronic myelomonocytic leukaemia Chronic Active Epstein-barr Virus infection (CAEBV) Chronic idiopathic myelofibrosis Chronic lymphocytic leukaemia Chronic myeloid leukaemia Chronic myeloid leukaemia, atypical Churg-Strauss CID CID with Ig CID with Immunoglobulins (CID with Ig) CIDP (Chronic inflammatory demyelinating polyneuropathy) CLL CLL/SLL, atypical CMML (Chronic myelomonocytic leukaemia) CMMoL (Chronic myelomonocytic leukaemia) CNS tumours Colon adenocarcinoma Combined myelodysplastic & myeloproliferative neoplasm Combined myelodysplastic & myeloproliferative syndromes Combined immune deficiency Common variable immunodeficiency (CID) Congenital neutropaenia (Kostmann syndrome) Congenital amegakaryocytosis Congenital PRCA Crohn s disease Crow-Fukase syndrome (POEMS) Cytopaenia Dermatomyositis Di George anomaly Diamond-Blackfan anaemia Diffuse large B-cell lymphoma Drepanocytosis Duncan syndrome (X-linked lymphoproliferative syndrome) Dyserythropoietic anaemia Dyskeratosis congenita EBV related lymphohistiocytosis (HLH) Embryonal carcinoma Enteropathy-type T-cell lymphoma Ependymoma Erythrophagocytic lympohystiocytosis/hemoph agocytosis Breast cancer Other LPD Hemoglobinopathy-other
3 Evan syndrome Ewing sarcoma Extranodal marginal zone of MALT type lymphoma Extranodal NK/T-cell lymphoma, nasal type Familial erythro/hemophagocytic lymphohistiocytosis (FELH) Familial reticuloendotheliosis (Omenn's syndrome) Fanconi anaemia FELH / FLH (Familial erythro / hemophagocytic lymphohistiocytosis) FHLH (Familial hemophagocytic lymphohistiocytosis) Fibrosarcoma Follicular lymphoma Follicular dendritic sarcoma Fucosidosis Gastric carcinoma + adenocarcinoma Gaucher disease Genetic agranulocytosis (Kostmann syndrome) Germ cell tumour Giant cell arteritis Glanzmann thrombasthenia Glioblastoma Globoid leukodystrophy (Krabbe disease) Glucose storage disease Granulocytic sarcoma Grave's disease Griscelli syndrome Haemoglobinopathy, heterozygous Hairy cell leukaemia Hairy Cell Leukaemia, atypic Hemangiosarcoma Hemolytic anemia, acquired Hemolytic anemia, congenital Hemolytic anemia, not congenital Hemophagocytosis (reactive or viral associated) Hepatosplenic gamma-delta T-cell lymphoma HGPRT deficiency (Lesch- Nyhan) Histiocytic sarcoma Histiocytosis X (Langerhans Cell Histiocytosis) HIV infection Hodgkin's Lymphoma Hunter syndrome (II) Hurler / Scheie syndrome Hurler syndrome (I) Hydroa Vacciniforme Hyper eosinophilic syndrome Hyper IgM syndrome (CD40 ligand deficiency) I-cell disease Idiopathic thrombocytopenic purpura (ITP) IL-7R alpha deficiency Immune deficiencies (primary) Immune deficiency with increased IgM (CD40 ligand deficiency) Inborn errors (except congenital BMF) Inborn errors of metabolism Inflammatory breast cancer Interferon gamma receptor deficiency ITP (Idiopathic thrombocytopenic purpura) JAK3 deficiency J (Juvenile myelomonocytic leukaemia) Ewing Germ cell tumor Others Hemoglobinopathy-other BM failure-other Langerhans cell histiocytosis Hodgkin Lymphoma Others Breast cancer
4 JCMML (Juvenile myelomonocytic leukaemia) JIA (Juvenile idiopathic arthritis) JMML (Juvenile myelomonocytic leukaemia) Juvenile myelomonocytic leukaemia Juvenile idiopathic arthritis (JIA) Kahler disease Kidney tumour (non Wilms) Kostmann syndrome Krabbe disease (globoid leukodystrophy) LAD (Leukocyte adhesion deficiency) Langerhans Cell Histiocytosis (Histiocytosis-X) Leiomyosarcoma Lennert lymphoma Lesch-Nyhan (HGPRT deficiency) Leukocyte adhesion deficiency (LAD) LFA deficiency (Leukocyte adhesion deficiency) Liposarcoma Louis-Bar Syndrome (Ataxia telangiectasia) Lung cancer, non-small cell Lung cancer, small cell Lymphoplasmacytic lymphoma Malignant histiocytosis MALT (Extranodal marginal zone of MALT type lymphoma) Mannosidosis Mantle cell lymphoma Marchiafava-Micheli syndrome Maroteaux-Lamy (VI) Mastocytosis, systemic MDS Mediastinal neoplasm Medulloblastoma Melanoma Metachromatic leukodystrophy MHC class II-deficiency Mixed tumour with seminoma Mixed tumour without seminoma Morquio (IV) MPS (not Mucopolysaccharidosis) MS (Multiple Sclerosis) Mucolipidoses Mucolipidoses II Mucopolysaccharidosis Multiple myeloma Multiple Sclerosis (MS) Myasthenia gravis Mycosis fungoides Myelodysplastic syndrome Myelodysplastic & myeloproliferative neoplasm combined Myelodysplastic & myeloproliferative syndromes combined Myelofibrosis with myeloid metaplasia (Chronic idiopathic myelofibrosis) Myeloproliferative neoplasm Myeloproliferative syndrome Myelosclerosis (Chronic idiopathic myelofibrosis) Necrotising arteritis Neuroblastoma Neurogenic sarcoma Neuronal ceriod lipofuscinosis (Batten disease) Langerhans cell histiocytosis Others Neuroblastoma
5 Neutrophil actin deficiency Nezelof syndrome (CID with Ig) NHL (Non Hodgkins Lymphoma) Niemann-Pick disease Nijmegen syndrome Nodal marginal zone B-cell lymphoma Non Hodgkins Lymphoma, unspecified Non inflammatory breast cancer Non-small cell lung cancer NSCLC Oligodendroglioma Omenn's syndrome Osteopetrosis Osteosarcoma Other (non Wilms) kidney tumour Other gliomas Ovarian adenocarcinoma Overlapping necrotising arteritis Paroxysmal nocturnal hemoglobinuria () PEP syndrome (POEMS) Peripheral T-cell Plasma cell disorders Plasma cell leukemia Platelet defect, congenital PLL PNET PNP- SCID POEMS syndrome Polyarteritis nodosa Polycythemia vera Polymyositis Polysaccharide hydrolase abnormalities Post-transplant lymphoproliferative disease PRCA (acquired) PRCA (congenital) PRCA (not congenital) Precursor B-lymphoblastic leukemia/lymphoma Precursor T-lymphoblastic lymphoma/leukemia Primary amyloidosis Prolymphocytic Leukaemia Prolymphocytic Leukaemia B- cell Prolymphocytic Leukaemia T- cell Psoriatic arthritis/psoriasis PTLD Pure red cell, acquired Pure white cell, acquired Purine nucleoside phosphorylase deficiency (SCID) (PNP-) Purtilo (X-linked lymphoproliferative syndrome) PWC (acquired) PWC (genetic) Pyruvate kinase deficiency resulting in hemolytic anaemia, congenital Rag-1 or Rag-2 Refractory anaemia (RA) Reticular dysgenesis (SCID) Retinoblastoma Rhabdomyosarcoma Rheumatoid arthritis Breast cancer Other LPD Aquired pure red cell anemia Aquired pure red cell anemia Lymphoblastic Lymphoma Lymphoblastic Lymphoma Other LPD Aquired pure red cell anemia BM failure-other
6 Richter Sanfilippo (III) Sarcoma not otherwise specified Sarcoma PNET Scheie syndrome (IS) SCID SCLC Scleroderma (Systemic sclerosis) Diagnosis Secondary acute leukaemia after MDS Secondary acute leukaemia after MPS Secondary acute leukaemia, after treatment of primary disease Seemanova syndrome Seminoma Severe combined immune deficiency (SCID) Severe congenital neutropenia (SCN) Severe mosquito bite allergy Sezary syndrome Shwachman-Diamond Sickle cell disease Sjögren syndrome SLE (Systemic lupus erythematosus) SLL Small cell lung cancer Small lymphocytic lymphoma Soft tissue sarcoma (include PNET sarcoma) Solid tumour Solitary plasmacytoma Sphingolipidoses Splenic marginal zone B-cell lymphoma Stills disease Subcutaneous panniculitis- like T-cell lymphoma Synovial sarcoma Systemic mastocytosis Systemic lupus erythematosus (SLE) Systemic sclerosis Takatsuki disease (POEMS) Takayasu T-cell granular lymphocytic leukaemia T-cell lymphomas (NHL), unspecified Teratocarcinoma Thalassemia Thrombocythemia (essential / primary) Thymoma T-lymphocyte deficiency (CID with Ig) Ulcerative colitis Undifferentiated carcinoma Waldenstrom Wegener granulomatosis Wilm tumour Wiskott Aldrich syndrome (XL) Wolman disease X-linked lymphoproliferative syndrome XLP (X-linked lymphoproliferative syndrome) Yolk sac tumour Hemoglobinopathy-other Hemoglobinopathy-Thalassemia
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