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... > Nutritional and Metabolic Diseases > Metabolic Diseases > Lipid Metabolism Disorders > Lipid Metabolism, Inborn Errors > Lipidoses > Sphingolipidoses > Niemann-Pick Diseases > Niemann-Pick Disease, Type B
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Lipid Metabolism, Inborn Errors > Lipidoses > Sphingolipidoses > Niemann-Pick Diseases > Niemann-Pick Disease, Type B
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Lipid Metabolism, Inborn Errors > Lipidoses > Sphingolipidoses > Niemann-Pick Diseases > Niemann-Pick Disease, Type B
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Brain Diseases, Metabolic > Brain Diseases, Metabolic, Inborn > Lysosomal Storage Diseases, Nervous System > Sphingolipidoses > Niemann-Pick Diseases > Niemann-Pick Disease, Type B
... > Nervous System Diseases > Central Nervous System Diseases > Brain Diseases > Brain Diseases, Metabolic > Brain Diseases, Metabolic, Inborn > Lysosomal Storage Diseases, Nervous System > Sphingolipidoses > Niemann-Pick Diseases > Niemann-Pick Disease, Type B
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Brain Diseases, Metabolic, Inborn > Lysosomal Storage Diseases, Nervous System > Sphingolipidoses > Niemann-Pick Diseases > Niemann-Pick Disease, Type B
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Brain Diseases, Metabolic, Inborn > Lysosomal Storage Diseases, Nervous System > Sphingolipidoses > Niemann-Pick Diseases > Niemann-Pick Disease, Type B
... > Congenital, Hereditary, and Neonatal Diseases and Abnormalities > Genetic Diseases, Inborn > Metabolism, Inborn Errors > Lysosomal Storage Diseases > Lysosomal Storage Diseases, Nervous System > Sphingolipidoses > Niemann-Pick Diseases > Niemann-Pick Disease, Type B
... > Nutritional and Metabolic Diseases > Metabolic Diseases > Metabolism, Inborn Errors > Lysosomal Storage Diseases > Lysosomal Storage Diseases, Nervous System > Sphingolipidoses > Niemann-Pick Diseases > Niemann-Pick Disease, Type B
... > Hemic and Lymphatic Diseases > Lymphatic Diseases > Histiocytosis > Histiocytosis, Non-Langerhans-Cell > Niemann-Pick Diseases > Niemann-Pick Disease, Type B

Término preferido

Niemann-Pick Disease, Type B  

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Tipo

  • mesh:Descriptor

Definición

  • An allelic disorder of TYPE A NIEMANN-PICK DISEASE, a late-onset form. It is also caused by mutation in SPHINGOMYELIN PHOSPHODIESTERASE but clinical signs involve only visceral organs (non-neuropathic type).

Concepto genérico

Etiquetas alternativas

  • Niemann-Pick Disease, Non-Neuronopathic Type
  • Niemann-Pick Disease, Visceral
  • Niemann-Pick's Disease Type B
  • Type B Niemann-Pick Disease

En otras lenguas

  • Maladie de Niemann-Pick de type B

    francés

  • Déficit en sphingomyélinase acide de type B
  • Maladie de Niemann-Pick non neuronopathique
  • Maladie de Niemann-Pick type B

URI

http://data.loterre.fr/ark:/67375/JVR-VSGZL4N5-J

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