Structured Summary
Abstract
Inborn errors of metabolism characterized by defects in specific lysosomal hydrolases and resulting in intracellular accumulation of unmetabolized substrates.
MeSH Record
Classification
Related Concepts
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MeSH Record
Synonyms
9 entry terms
- Lysosomal Enzyme Disorders
- Disease, Lysosomal Storage
- Diseases, Lysosomal Storage
- Disorder, Lysosomal Enzyme
- Disorders, Lysosomal Enzyme
- Enzyme Disorder, Lysosomal
- Enzyme Disorders, Lysosomal
- Lysosomal Enzyme Disorder
- Lysosomal Storage Disease
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
an inborn error of metab; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
MeSH Record
History Note
92
MeSH Record
Previous Indexing
- Metabolism, Inborn Errors (1972-1991)
MeSH Hierarchy
Tree Numbers
MeSH Record
NLM Classification
QU 265.5.L9
AMA Style
References
- National Library of Medicine. Lysosomal Storage Diseases. Medical Subject Headings (MeSH). 2026. Unique ID D016464. http://id.nlm.nih.gov/mesh/2026/D016464
- Lysosomal Storage Diseases. In: Wikipedia. https://en.wikipedia.org/wiki/Lysosomal_storage_disease
- Lysosomal Storage Diseases. In: Wikidata. https://www.wikidata.org/wiki/Q675010