Busulfan

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Nume		Busulfan

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Boli A-Z		46 Xx Gonadal Dysgenesis Acquired Idiopathic Sideroblastic Anemia Acquired Immunodeficiency Syndrome Acute Basophilic Leukemia Acute Biphenotypic Leukemia Acute Erythroid Leukemia Acute Graft Versus Host Disease Acute Leukemia Acute Leukemia of Ambiguous Lineage Acute Lymphoblastic Leukemia, Childhood Acute Lymphocytic Leukemia Acute Monoblastic Leukemia Acute Myeloblastic Leukemia with Maturation Acute Myeloblastic Leukemia Without Maturation Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) Acute Myeloid Leukemia with Minimal Differentiation Acute Non Lymphoblastic Leukemia Acute Promyelocytic Leukemia Acute T Cell Leukemia Adenocarcinoma Adenosine Deaminase Deficiency Adrenal Cortical Hypofunction Adrenal Gland Disease Adrenoleukodystrophy Adrenomyeloneuropathy Adult Acute Lymphocytic Leukemia Adult Acute Monocytic Leukemia Adult Neuronal Ceroid Lipofuscinosis Adult Oligodendroglioma Adult T-Cell Leukemia Agammaglobulinemia Agammaglobulinemia, X-Linked Al Amyloidosis Alopecia Alopecia Areata Alpha-Methylacyl-Coa Racemase Deficiency Amegakaryocytic Thrombocytopenia, Congenital Aml with Myelodysplasia-Related Features Amyloidosis Anaplastic Large Cell Lymphoma Anaplastic Oligodendroglioma Angioimmunoblastic Lymphadenopathy with Dysproteinemia Angioimmunoblastic T-Cell Lymphoma Anxiety Aphasia Aplastic Anemia Arachnoiditis Aregenerative Anemia Aseptic Meningitis Aspartylglucosaminuria Astrocytoma Atypical Chronic Myeloid Leukemia Atypical Teratoid Rhabdoid Tumor Autism X-Linked 2 Autoimmune Disease B- and T-Cell Mixed Leukemia Bare Lymphocyte Syndrome, Type Ii B-Cell Childhood Acute Lymphoblastic Leukemia B-Cell Growth Factor B-Cell Lymphomas Beta-Thalassemia Bladder Cancer Bladder Disease Blood Coagulation Disease Blood Platelet Disease Bone Cancer Bone Marrow Cancer Bone Osteosarcoma Brain Cancer Brain Stem Glioma Brain Tumor, Childhood Breast Cancer Breast Disease Brittle Bone Disorder Bronchus Cancer Burkitt Lymphoma Capillary Disease Carbohydrate Metabolic Disorder Carcinoma Showing Thymus-Like Differentiation Cataract Cd40 Ligand Deficiency Central Nervous System Disease Central Nervous System Germ Cell Tumor Central Nervous System Leukemia Central Nervous System Lymphoma Cerebellar Astrocytoma Cerebellar Astrocytoma, Childhood Cerebellar Degeneration-Related Autoantigen 3 Ceroid Lipofuscinosis, Neuronal, 3 Ceroid Lipofuscinosis, Neuronal, 4a, Autosomal Recessive Ceroid Storage Disease Charcot-Marie-Tooth Disease Charcot-Marie-Tooth Hereditary Neuropathy Chediak-Higashi Syndrome Childhood Brain Stem Glioma Childhood Cerebral Astrocytoma Childhood Choroid Plexus Cancer Childhood Kidney Cell Carcinoma Childhood Medulloblastoma Childhood Oligodendroglioma Childhood Optic Nerve Glioma Cholesterol Ester Storage Disease Chordoma Chromosomal Disease Chromosome 12p Deletion Chromosome 1p Deletion Chronic Eosinophilic Leukemia Chronic Graft Versus Host Disease Chronic Granulomatous Disease Chronic Leukemia Chronic Myelomonocytic Leukemia Chronic Neutrophilic Leukemia Classic Hairy Cell Leukemia Clear Cell Adenocarcinoma Clear Cell Adenoma Clear Cell Renal Cell Carcinoma Cll/sll Cln4 Disease Collagen Disease Combined Immunodeficiency, X-Linked Common Variable Immunodeficiency Complement Deficiency Congenital Hypoplastic Anemia Congenital Short Bowel Syndrome Congestive Heart Failure Connective Tissue Cancer Connective Tissue Disease Core Binding Factor Acute Myeloid Leukemia Cranial Nerve Disease Cutaneous T Cell Lymphoma Cystitis Cytomegalic Inclusion Disease Cytomegalovirus Infection D-Bifunctional Protein Deficiency Dementia Demyelinating Disease Desmoplastic Small Round Cell Tumor Diamond-Blackfan Anemia Diarrhea Diffuse Large B-Cell Lymphoma Diffuse Scleroderma Disseminated Eosinophilic Collagen Disease Down Syndrome Dysgammaglobulinemia Dyskeratosis Congenita Encephalomyopathy Encephalopathy Endemic Typhus Enthesopathy Ependymoma Epidermolysis Bullosa Epidermolysis Bullosa Dystrophica Epidermolysis Bullosa Dystrophica, Autosomal Recessive Epithelial-Myoepithelial Carcinoma Erythema Elevatum Diutinum Essential Thrombocythemia Estrogen-Receptor Negative Breast Cancer Estrogen-Receptor Positive Breast Cancer Ewing's Family of Tumors Ewing Sarcoma Exanthem Exocrine Pancreatic Insufficiency Extragonadal Germ Cell Cancer Extragonadal Nonseminomatous Germ Cell Tumor Extramedullary Plasmacytoma Extranodal Nasal Nk/t Cell Lymphoma Extraocular Retinoblastoma Factor Xi Deficiency Fanconi Anemia, Complementation Group a Fanconi Syndrome Follicular Lymphoma Fox-Fordyce Disease Frontotemporal Dementia Frontotemporal Dementia with Parkinsonism-17 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related Fucosidosis Ganglioneuroblastoma Gangliosidosis Gm1 Gaucher's Disease Gaucher Disease, Type I Genitourinary Tract Anomalies Germ Cells Tumors Gestational Trophoblastic Neoplasm Gestational Trophoblastic Tumor Giant Cell Glioblastoma Glanzmann Thrombasthenia Glioblastoma Glioblastoma Multiforme Glioma Gliosarcoma Gm1-Gangliosidosis, Type I Gonadal Disease Gonadal Dysgenesis Gout Grade Iii Astrocytoma Graft-Versus-Host Disease Granulocytopenia Granulomatous Disease, Chronic, X-Linked Griscelli Syndrome Grn-Related Frontotemporal Dementia Hair Whorl Hairy Cell Leukemia Heart Cancer Hematologic Cancer Hematopoietic Stem Cell Transplantation Hemoglobin C Disease Hemoglobinopathy Hemoglobinuria Hemophagocytic Lymphohistiocytosis Hemophagocytic Lymphohistiocytosis, Familial, 1 Hemorrhagic Cystitis Hemorrhagic Disease Hemosiderosis Hepatic Veno-Occlusive Disease Hepatitis Hepatitis a Hepatoblastoma Hepatosplenic T-Cell Lymphoma Hereditary Neuropathy with Liability to Pressure Palsy Histiocytosis Hodgkin's Granuloma Hodgkin's Paragranuloma Hodgkin Lymphoma, Childhood Homologous Wasting Disease Human Immunodeficiency Virus Type 1 Hurler Syndrome Hypereosinophilic Syndrome Hypereosinophilic Syndrome, Idiopathic Hyper-Ige Recurrent Infection Syndrome, Autosomal Recessive Hypoadrenalism Immune Deficiency Disease Immune Suppression Immune System Disease Immunodeficiency 21 Immunodeficiency with Hyper-Igm, Type 1 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked Immunoerythromyeloid Hypoplasia Inclusion-Cell Disease Infertility Inflammatory Breast Carcinoma Influenza Inherited Blood Coagulation Disease Inherited Bone Marrow Failure Syndromes Inherited Metabolic Disorder Interdigitating Dendritic Cell Sarcoma Intestinal Disease Intestinal Obstruction Intestinal Pseudo-Obstruction Intraocular Lymphoma Intraocular Retinoblastoma Juvenile Myelomonocytic Leukemia Kidney Cancer Kidney Disease Krabbe Disease Langerhans Cell Histiocytosis Large Granular Lymphocyte Leukemia Lethal Midline Granuloma Letterer-Siwe Disease Leukemia Leukemia, Acute Lymphoblastic Leukemia, Acute Monocytic Leukemia, Acute Myeloid Leukemia, B-Cell, Chronic Leukemia, Chronic Lymphocytic Leukemia, Chronic Lymphocytic 2 Leukemia, Chronic Lymphocytic 3 Leukemia, Chronic Myeloid Leukemia, T-Cell, Chronic Leukocyte Adhesion Deficiency, Type I Leukocyte Disease Leukodystrophy Lipid Metabolism Disorder Lipid Storage Disease Lipomatosis Liver Disease Lung Cancer Lung Disease Lung Squamous Cell Carcinoma Lupus Erythematosus Lymphatic System Disease Lymphoblastic Leukemia Lymphoblastic Lymphoma Lymphoid Leukemia Lymphoma Lymphoma Aids Related Lymphoma, Hodgkin, Classic Lymphoma, Large-Cell, Immunoblastic Lymphoma, Mucosa-Associated Lymphoid Type Lymphoma, Non-Hodgkin, Familial Lymphoma, Small Cleaved-Cell, Diffuse Lymphomatoid Granulomatosis Lymphomatous Meningitis Lymphopenia Lymphoplasmacyte-Rich Meningioma Lymphoplasmacytic Lymphoma Lymphoproliferative Syndrome Lymphoproliferative Syndrome, X-Linked, 1 Lymphosarcoma Lysosomal Acid Lipase Deficiency Lysosomal Storage Disease Macroglobulinemia Macrophage Activation Syndrome Malignant Germ Cell Tumor Malignant Glioma Malignant Mesenchymoma Mannosidosis Mannosidosis, Alpha B, Lysosomal Mantle Cell Lymphoma Marginal Zone B-Cell Lymphoma Mast Cell Activation Syndrome Mast Cell Disease Mast-Cell Leukemia Maturity-Onset Diabetes of the Young Medulloblastoma Megakaryocytic Leukemia Melanoma Meningitis Metachromatic Leukodystrophy Mirage Syndrome Mitochondrial Disorders Mitochondrial Dna Depletion Syndrome 1 Mitochondrial Encephalomyopathy Mitochondrial Myopathy Mitochondrial Neurogastrointestinal Encephalopathy Disease Mixed Germ Cell Tumor Mixed Glioma Monoclonal Gammopathy of Uncertain Significance Monocytic Leukemia Morquio Syndrome Motor Peripheral Neuropathy Mucinoses Mucolipidoses Mucolipidosis Ii Alpha/beta Mucolipidosis Iv Mucopolysaccharidoses Mucopolysaccharidosis Iv Mucopolysaccharidosis, Type Ii Mucopolysaccharidosis Type Vi Mucopolysaccharidosis, Type Vii Mucositis Multiple Sclerosis Muscle Cancer Muscle Disorders Muscle Tissue Disease Mycosis Fungoides Myelodysplastic Myeloproliferative Cancer Myelodysplastic Syndrome Myelofibrosis Myeloid Leukemia Myeloid Sarcoma Myeloma, Multiple Myeloproliferative Neoplasm Myeloproliferative Syndrome, Transient Myoma Myopathy Myopia Neonatal Adrenoleukodystrophy Nerve Compression Syndrome Nervous System Cancer Nervous System Disease Neuritis Neuroblastoma Neuroendocrine Tumor Neuromuscular Disease Neuronal Ceroid-Lipofuscinoses Neuronal Ceroid Lipofuscinosis Neuropathy Neuropathy, Hereditary, with Liability to Pressure Palsies Neutropenia Neutropenia, Severe Congenital, 3, Autosomal Recessive Niemann-Pick Disease Niemann-Pick Disease, Type a Niemann-Pick Disease, Type B Nodal Marginal Zone B-Cell Lymphoma Noninvasive Malignant Thymoma Non-Langerhans-Cell Histiocytosis Nonseminomatous Germ Cell Tumor Ocular Cancer Oculocerebral Syndrome with Hypopigmentation Oligodendroglioma Omenn Syndrome Optic Nerve Disease Optic Nerve Glioma Optic Nerve Neoplasm Optic Pathway Glioma Osteochondrodysplasia Osteogenesis Imperfecta, Type Ii Osteogenesis Imperfecta, Type Iii Osteogenic Sarcoma Osteopetrosis Ovarian Cancer Ovarian Cancer 1 Ovarian Disease Ovarian Epithelial Cancer Ovarian Germ Cell Cancer Ovarian Mixed Germ Cell Neoplasm Pancreas Disease Pancytopenia Parotitis Paroxysmal Nocturnal Hemoglobinuria Pediatric Ependymoma Pediatric Extraocular Retinoblastoma Pediatric Germ Cell Cancer Pediatric Infratentorial Ependymoma Pediatric Intraocular Retinoblastoma Pediatric Supratentorial Ependymoma Peripheral Nervous System Disease Peripheral Nervous System Neoplasm Peripheral T-Cell Lymphoma Peroxisomal Acyl-Coa Oxidase Deficiency Peroxisomal Biogenesis Disorders Peroxisomal Disease Peroxisome Biogenesis Disorder 1b Peroxisome Disorders Phagocyte Bactericidal Dysfunction Pharyngitis Pick Disease of Brain Pineal Gland Cancer Pineal Region Germinoma Pineoblastoma Pineoblastoma, Childhood Pineocytoma Plasmablastic Lymphoma Plasma Cell Leukemia Plasma Cell Neoplasm Plasmacytic Leukemia Plasmacytoma Polycythemia Polycythemia Vera Polyneuropathy Post-Transplant Lymphoproliferative Disease Primary Central Nervous System Lymphoma Primary Effusion Lymphoma Primary Fanconi Syndrome Primary Polycythemia Primary Progressive Apraxia of Speech Progesterone-Receptor Negative Breast Cancer Progesterone-Receptor Positive Breast Cancer Prolymphocytic Leukemia Psoriasis Pulmonary Fibrosis Pure Red-Cell Aplasia Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia Recessive Dystrophic Epidermolysis Bullosa Refractory Anemia Refractory Anemia with Excess Blasts Refractory Anemia with Excess Blasts in Transformation Refractory Hairy Cell Leukemia Refractory Hematologic Cancer Refractory Plasma Cell Neoplasm Refsum Disease, Classic Refsum Disease, Infantile Form Renal Cell Carcinoma, Nonpapillary Renal Clear Cell Carcinoma Renal Tubular Transport Disease Reticular Dysgenesis Reticulosarcoma Reticulum Cell Sarcoma Retinal Cancer Retinal Disease Retinoblastoma Rhabdoid Cancer Rhabdoid Tumor Predisposition Syndrome 1 Rhabdoid Tumor Predisposition Syndrome 2 Rhabdomyosarcoma Rheumatic Disease Rigid Spine Muscular Dystrophy 1 Roussy-Levy Hereditary Areflexic Dystasia Sandhoff Disease Sarcoma Scleroderma, Familial Progressive Scoliosis, Isolated 1 Secretory Meningioma Semantic Dementia Severe Combined Immunodeficiency Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency Severe Combined Immunodeficiency, X-Linked Severe Congenital Neutropenia Sex Differentiation Disease Sezary's Disease Shwachman-Diamond Syndrome Sickle Beta Thalassemia Sickle Cell Anemia Sickle Cell Disease Skeletal Dysplasias Skin Conditions Skin Disease Skin Melanoma Sleep Disorder Small Intestine Lymphoma Small Non-Cleaved Cell Lymphoma Soft Tissue Sarcoma Solitary Osseous Plasmacytoma Spastic Diplegia Speech and Communication Disorders Speech Disorder Sphingolipidosis Spinal Arachnoiditis Splenic Marginal Zone Lymphoma Splenomegaly Stomatitis Sudanophilic Cerebral Sclerosis Supratentorial Primitive Neuroectodermal Tumor Supratentorial Primitive Neuroectodermal Tumors, Childhood Syndactyly, Type Iv Systemic Lupus Erythematosus Systemic Scleroderma Tay-Sachs Disease T-Cell Adult Acute Lymphocytic Leukemia T-Cell Childhood Acute Lymphocytic Leukemia T Cell Immunodeficiency Primary T-Cell Large Granular Lymphocyte Leukemia T-Cell Leukemia T-Cell Prolymphocytic Leukemia Teratoma Testicular Cancer Testicular Disease Testicular Germ Cell Cancer Testicular Germ Cell Tumor Testicular Leukemia Testicular Lymphoma Thalassemia Thrombasthenia Thrombocytopenia Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenic Purpura, Autoimmune Thrombocytosis Thrombosis Thymoma Thymus Cancer Toxic Encephalopathy Transitional Cell Carcinoma Trichohepatoenteric Syndrome 1 Trichohepatoenteric Syndrome 2 Trophoblastic Neoplasm Turner Syndrome Type C Thymoma Urinary System Disease Vascular Disease Vascular Hemostatic Disease Vesiculobullous Skin Disease Viral Hepatitis Viral Infectious Disease Virus Associated Hemophagocytic Syndrome Waldenstrom Macroglobulinemia Wegener Granulomatosis Werner Syndrome Wilms Tumor 1 Wilms Tumor 5 Wiskott-Aldrich Syndrome Zellweger Syndrome