Lipid Metabolism, Inborn Errors

Errors in the metabolism of LIPIDS resulting from inborn genetic MUTATIONS that are heritable.

Year introduced: 1965

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

Tree Number(s): C16.320.565.398, C18.452.584.563, C18.452.648.398

MeSH Unique ID: D008052

Entry Terms:

• Lipid Metabolism, Inborn Error

All MeSH Categories
Diseases Category
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Barth Syndrome
Hyperlipidemia, Familial Combined
Hyperlipoproteinemia Type I
Hyperlipoproteinemia Type II
Homozygous Familial Hypercholesterolemia
Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type IV
Hyperlipoproteinemia Type V
Hypolipoproteinemias
Hypoalphalipoproteinemias +
Hypobetalipoproteinemias +
Lipidoses
Cholesterol Ester Storage Disease +
Neuronal Ceroid-Lipofuscinoses
Sjogren-Larsson Syndrome
Sphingolipidoses +
Lipodystrophy, Congenital Generalized
Smith-Lemli-Opitz Syndrome
Xanthomatosis, Cerebrotendinous

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Lipid Metabolism, Inborn Errors
Barth Syndrome
Hyperlipidemia, Familial Combined
Hyperlipoproteinemia Type I
Hyperlipoproteinemia Type II
Homozygous Familial Hypercholesterolemia
Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type IV
Hyperlipoproteinemia Type V
Hypobetalipoproteinemia, Familial, Apolipoprotein B
Hypolipoproteinemias
Hypoalphalipoproteinemias +
Hypobetalipoproteinemias +
Lipidoses
Cholesterol Ester Storage Disease +
Neuronal Ceroid-Lipofuscinoses
Sjogren-Larsson Syndrome
Sphingolipidoses +
Lipodystrophy, Congenital Generalized
Lipodystrophy, Familial Partial
Shwachman-Diamond Syndrome
Smith-Lemli-Opitz Syndrome
Xanthomatosis, Cerebrotendinous

All MeSH Categories
Diseases Category
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Barth Syndrome
Hyperlipidemia, Familial Combined
Hyperlipoproteinemia Type I
Hyperlipoproteinemia Type II
Homozygous Familial Hypercholesterolemia
Hyperlipoproteinemia Type III
Hyperlipoproteinemia Type IV
Hyperlipoproteinemia Type V
Hypolipoproteinemias
Hypoalphalipoproteinemias +
Hypobetalipoproteinemias +
Lipidoses
Cholesterol Ester Storage Disease +
Neuronal Ceroid-Lipofuscinoses
Sjogren-Larsson Syndrome
Sphingolipidoses +
Lipodystrophy, Congenital Generalized
Smith-Lemli-Opitz Syndrome
Xanthomatosis, Cerebrotendinous