Structured Summary
Abstract
Errors in the metabolism of LIPIDS resulting from inborn genetic MUTATIONS that are heritable.
MeSH Record
Classification
Broader headings
Narrower headings
- Barth Syndrome
- Cerebrotendinous Xanthomatosis
- Congenital Generalized Lipodystrophy
- Familial Apolipoprotein B Hypobetalipoproteinemia
- Familial Combined Hyperlipidemia
- Familial Partial Lipodystrophy
- Hyperlipoproteinemia Type I
- Hyperlipoproteinemia Type II
- Hyperlipoproteinemia Type III
- Hyperlipoproteinemia Type IV
- Hyperlipoproteinemia Type V
- Hypolipoproteinemias
- Lipidoses
- Shwachman-Diamond Syndrome
- Smith-Lemli-Opitz Syndrome
Related Concepts
Knowledge Graph
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MeSH Record
Synonyms
2 entry terms
- Lipid Metabolism, Inborn Error
- Lipid Metabolism, Inborn Errors
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
Indexing Annotation
coordinate with specific lipid /metab
MeSH Record
History Note
65
MeSH Hierarchy
Tree Numbers
MeSH Record
NLM Classification
QU 265.5.L5
AMA Style
References
- National Library of Medicine. Inborn Errors Lipid Metabolism. Medical Subject Headings (MeSH). 2026. Unique ID D008052. http://id.nlm.nih.gov/mesh/2026/D008052
- Inborn Errors Lipid Metabolism. In: Wikipedia. https://en.wikipedia.org/wiki/Inborn_error_of_lipid_metabolism
- Inborn Errors Lipid Metabolism. In: Wikidata. https://www.wikidata.org/wiki/Q15051322