Categorias DeCS
A11 Cells .
A11.329 Connective Tissue Cells .
A11.329.372 Macrophages .
A11.329.372.385 Histiocytes .
A11.627 Myeloid Cells .
A11.627.482 Macrophages .
A11.627.482.385 Histiocytes .
A11.733 Phagocytes .
A11.733.397 Macrophages .
A11.733.397.385 Histiocytes .
A15 Hemic and Immune Systems .
A15.382 Immune System .
A15.382.680 Phagocytes .
A15.382.680.397 Macrophages .
A15.382.680.397.385 Histiocytes .
A15.382.812 Mononuclear Phagocyte System .
A15.382.812.522 Macrophages .
A15.382.812.522.385 Histiocytes .
C04 Neoplasms .
C04.557 Neoplasms by Histologic Type .
C04.557.450 Neoplasms, Connective and Soft Tissue .
C04.557.450.565 Neoplasms, Connective Tissue .
C04.557.450.565.590 Neoplasms, Fibrous Tissue .
C04.557.450.565.590.425 Histiocytoma .
C08 Respiratory Tract Diseases .
C08.381 Lung Diseases .
C08.381.483 Lung Diseases, Interstitial .
C08.381.483.375 Histiocytosis, Langerhans-Cell .
C10 Nervous System Diseases .
C10.228 Central Nervous System Diseases .
C10.228.140 Brain Diseases .
C10.228.140.163 Brain Diseases, Metabolic .
C10.228.140.163.100 Brain Diseases, Metabolic, Inborn .
C10.228.140.163.100.435 Lysosomal Storage Diseases, Nervous System .
C10.228.140.163.100.435.825 Sphingolipidoses .
C10.228.140.163.100.435.825.400 Gaucher Disease .
C10.228.140.163.100.435.825.700 Niemann-Pick Diseases .
C15 Hemic and Lymphatic Diseases .
C15.604 Lymphatic Diseases .
C15.604.250 Histiocytosis .
C15.604.250.400 Histiocytosis, Langerhans-Cell .
C15.604.250.410 Histiocytosis, Non-Langerhans-Cell .
C15.604.250.410.450 Histiocytosis, Sinus .
C15.604.250.410.625 Niemann-Pick Diseases .
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities .
C16.320 Genetic Diseases, Inborn .
C16.320.565 Metabolism, Inborn Errors .
C16.320.565.189 Brain Diseases, Metabolic, Inborn .
C16.320.565.189.435 Lysosomal Storage Diseases, Nervous System .
C16.320.565.189.435.825 Sphingolipidoses .
C16.320.565.189.435.825.400 Gaucher Disease .
C16.320.565.189.435.825.700 Niemann-Pick Diseases .
C16.320.565.398 Lipid Metabolism, Inborn Errors .
C16.320.565.398.641 Lipidoses .
C16.320.565.398.641.803 Sphingolipidoses .
C16.320.565.398.641.803.441 Gaucher Disease .
C16.320.565.398.641.803.730 Niemann-Pick Diseases .
C16.320.565.595 Lysosomal Storage Diseases .
C16.320.565.595.554 Lysosomal Storage Diseases, Nervous System .
C16.320.565.595.554.825 Sphingolipidoses .
C16.320.565.595.554.825.400 Gaucher Disease .
C16.320.565.595.554.825.700 Niemann-Pick Diseases .
C18 Nutritional and Metabolic Diseases .
C18.452 Metabolic Diseases .
C18.452.132 Brain Diseases, Metabolic .
C18.452.132.100 Brain Diseases, Metabolic, Inborn .
C18.452.132.100.435 Lysosomal Storage Diseases, Nervous System .
C18.452.132.100.435.825 Sphingolipidoses .
C18.452.132.100.435.825.400 Gaucher Disease .
C18.452.132.100.435.825.700 Niemann-Pick Diseases .
C18.452.584 Lipid Metabolism Disorders .
C18.452.584.687 Lipidoses .
C18.452.584.687.803 Sphingolipidoses .
C18.452.584.687.803.441 Gaucher Disease .
C18.452.584.687.803.730 Niemann-Pick Diseases .
C18.452.648 Metabolism, Inborn Errors .
C18.452.648.189 Brain Diseases, Metabolic, Inborn .
C18.452.648.189.435 Lysosomal Storage Diseases, Nervous System .
C18.452.648.189.435.825 Sphingolipidoses .
C18.452.648.189.435.825.400 Gaucher Disease .
C18.452.648.189.435.825.700 Niemann-Pick Diseases .
C18.452.648.398 Lipid Metabolism, Inborn Errors .
C18.452.648.398.641 Lipidoses .
C18.452.648.398.641.803 Sphingolipidoses .
C18.452.648.398.641.803.441 Gaucher Disease .
C18.452.648.398.641.803.730 Niemann-Pick Diseases .
C18.452.648.595 Lysosomal Storage Diseases .
C18.452.648.595.554 Lysosomal Storage Diseases, Nervous System .
C18.452.648.595.554.825 Sphingolipidoses .
C18.452.648.595.554.825.400 Gaucher Disease .
C18.452.648.595.554.825.700 Niemann-Pick Diseases .
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| | Termos Sinônimos e Históricos | Documentos LILACS e MDL | | | | | | | |
| Gaucher Disease . Acid beta-Glucosidase Deficiency . Acid beta-Glucosidase Deficiency Disease . Acute Neuronopathic Gaucher Disease . Chronic Gaucher Disease . GBA Deficiency . Gaucher Disease Type 3 . Gaucher Disease, Acute Neuronopathic . Gaucher Disease, Acute Neuronopathic Type . Gaucher Disease, Chronic . Gaucher Disease, Chronic Neuronopathic Type . Gaucher Disease, Infantile . Gaucher Disease, Infantile Cerebral . Gaucher Disease, Juvenile . Gaucher Disease, Juvenile and Adult, Cerebral . Gaucher Disease, Neuronopathic . Gaucher Disease, Non-Neuronopathic Form . Gaucher Disease, Noncerebral Juvenile . Gaucher Disease, Subacute Neuronopathic Form . Gaucher Disease, Subacute Neuronopathic Type . Gaucher Disease, Type 1 . Gaucher Disease, Type 2 . Gaucher Disease, Type 3 . Gaucher Disease, Type I . Gaucher Disease, Type II . Gaucher Disease, Type III . Gaucher Splenomegaly . Gaucher Syndrome . Gaucher's Disease . Gauchers Disease . Glucocerebrosidase Deficiency . Glucocerebrosidosis . Glucosyl Cerebroside Lipidosis . Glucosylceramidase Deficiency . Glucosylceramide Beta-Glucosidase Deficiency . Glucosylceramide Lipidosis . Infantile Gaucher Disease . Kerasin Histiocytosis . Kerasin Lipoidosis . Kerasin thesaurismosis . Lipoid Histiocytosis (Kerasin Type) . Non-Neuronopathic Gaucher Disease . Subacute Neuronopathic Gaucher Disease . Type 1 Gaucher Disease . Type 2 Gaucher Disease . Type 3 Gaucher Disease . Cerebroside Lipidoses, Glucosyl . Cerebroside Lipidosis Syndromes . Cerebroside Lipidosis, Glucosyl . Deficiencies, GBA . Deficiencies, Glucocerebrosidase . Deficiency Disease, Glucocerebrosidase . Deficiency Diseases, Glucocerebrosidase . Deficiency, GBA . Deficiency, Glucocerebrosidase . Disease, Chronic Gaucher . Disease, Gaucher . Disease, Gaucher's . Disease, Gauchers . Disease, Glucocerebrosidase Deficiency . Disease, Infantile Gaucher . Disease, Juvenile Gaucher . Disease, Neuronopathic Gaucher . Disease, Non-Neuronopathic Gaucher . Diseases, Gauchers . Diseases, Glucocerebrosidase Deficiency . GBA Deficiencies . Gaucher Disease, Non Neuronopathic Form . Gaucher Disease, Non-Neuronopathic . Gauchers Diseases . Glucocerebrosidase Deficiencies . Glucocerebrosidase Deficiency Diseases . Glucocerebrosidoses . Glucosyl Cerebroside Lipidoses . Glucosylceramide Lipidoses . Histiocytoses, Kerasin . Histiocytoses, Lipoid (Kerasin Type) . Histiocytosis, Kerasin . Histiocytosis, Lipoid (Kerasin Type) . Juvenile Gaucher Disease . Kerasin Histiocytoses . Kerasin Lipoidoses . Kerasin thesaurismoses . Lipidoses, Glucosyl Cerebroside . Lipidoses, Glucosylceramide . Lipidosis Syndrome, Cerebroside . Lipidosis Syndromes, Cerebroside . Lipidosis, Glucosyl Cerebroside . Lipidosis, Glucosylceramide . Lipoid Histiocytoses (Kerasin Type) . Lipoidoses, Kerasin . Lipoidosis, Kerasin . Non Neuronopathic Gaucher Disease . Splenomegaly, Gaucher . Syndrome, Cerebroside Lipidosis . Syndrome, Gaucher . Syndromes, Cerebroside Lipidosis . thesaurismoses, Kerasin . thesaurismosis, Kerasin . Cerebroside Lipidosis Syndrome . Glucocerebrosidase Deficiency Disease . Glucosylceramide Beta-Glucosidase Deficiency Disease . Neuronopathic Gaucher Disease . Gaucher Disease Type 1 . Gaucher Disease Type 2 . GAUCHER'S DISEASE . 0.66
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| Histiocytosis, Langerhans-Cell . Hand-Schueller-Christian Disease . Hand-Schueller-Christian Syndrome . Hand-Schüller-Christian Disease . Hand-Schüller-Christian Syndrome . Hashimoto-Pritzger Disease . Histiocytosis, Generalized . Histiocytosis-X . Langerhans Cell Granulomatosis . Langerhans Cell Granulomatosis, Pulmonary . Langerhans Cell Histiocytosis . Letterer-Siwe Disease . Non-Lipid Reticuloendotheliosis . Pulmonary Histiocytosis X . Pulmonary Langerhans Cell Granulomatosis . Schueller-Christian Disease . Systemic Aleukemic Reticuloendotheliosis . Type 2 Histiocytosis . Aleukemic Reticuloendothelioses, Systemic . Aleukemic Reticuloendotheliosis, Systemic . Cell Granulomatoses, Langerhans . Cell Granulomatosis, Langerhans . Cell Histiocytoses, Langerhans . Cell Histiocytosis, Langerhans . Disease, Hand-Schueller-Christian . Disease, Hand-Schüller-Christian . Disease, Letterer-Siwe . Disease, Schueller-Christian . Generalized Histiocytoses . Generalized Histiocytosis . Granulomatoses, Langerhans Cell . Granulomatosis, Langerhans Cell . Granulomatosis, Langerhans-Cell . Hand Schueller Christian Disease . Hand Schueller Christian Syndrome . Hand Schüller Christian Disease . Hand Schüller Christian Syndrome . Histiocytoses, Generalized . Histiocytoses, Langerhans Cell . Histiocytoses, Type 2 . Histiocytosis X, Pulmonary . Histiocytosis, Langerhans Cell . Histiocytosis, Type 2 . Langerhans Cell Granulomatoses . Langerhans Cell Histiocytoses . Letterer Siwe Disease . Non Lipid Reticuloendotheliosis . Non-Lipid Reticuloendothelioses . Reticuloendothelioses, Non-Lipid . Reticuloendothelioses, Systemic Aleukemic . Reticuloendotheliosis, Non-Lipid . Reticuloendotheliosis, Systemic Aleukemic . Schueller Christian Disease . Syndrome, Hand-Schueller-Christian . Syndrome, Hand-Schüller-Christian . Systemic Aleukemic Reticuloendothelioses . Type 2 Histiocytoses . Histiocytosis X . Langerhans-Cell Granulomatosis . Langerhans-Cell Histiocytosis . Hand-Schueller-Christian Syndrome . Schueller-Christian Disease . Letterer-Siwe Disease . Histiocytosis, Generalized . 0.63
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