Lipidoses

Conditions characterized by abnormal lipid deposition due to disturbance in lipid metabolism, such as hereditary diseases involving lysosomal enzymes required for lipid breakdown. They are classified either by the enzyme defect or by the type of lipid involved.

Year introduced: 2007 (1966)

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Do not include MeSH terms found below this term in the MeSH hierarchy.

Tree Number(s): C16.320.565.398.641, C18.452.584.563.641, C18.452.648.398.641

MeSH Unique ID: D008064

Entry Terms:

• Lipoidosis
• Lipidosis

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Lipidoses
Cholesterol Ester Storage Disease
Wolman Disease
Neuronal Ceroid-Lipofuscinoses
Sjogren-Larsson Syndrome
Sphingolipidoses
Fabry Disease
Farber Lipogranulomatosis
Gangliosidoses +
Gaucher Disease
Leukodystrophy, Globoid Cell
Niemann-Pick Diseases +
Sea-Blue Histiocyte Syndrome
Sulfatidosis +

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Lipid Metabolism, Inborn Errors
Lipidoses
Cholesterol Ester Storage Disease
Wolman Disease
Neuronal Ceroid-Lipofuscinoses
Sjogren-Larsson Syndrome
Sphingolipidoses
Fabry Disease
Farber Lipogranulomatosis
Gangliosidoses +
Gaucher Disease
Leukodystrophy, Globoid Cell
Niemann-Pick Diseases +
Sea-Blue Histiocyte Syndrome
Sulfatidosis +

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Lipidoses
Cholesterol Ester Storage Disease
Wolman Disease
Neuronal Ceroid-Lipofuscinoses
Sjogren-Larsson Syndrome
Sphingolipidoses
Fabry Disease
Farber Lipogranulomatosis
Gangliosidoses +
Gaucher Disease
Leukodystrophy, Globoid Cell
Niemann-Pick Diseases +
Sea-Blue Histiocyte Syndrome
Sulfatidosis +