lipid storage disease
Sign in to saveAlso known as inborn error of lipid storage, inborn lipid storage disorder, lipoid storage diseas, lipidoses, lipoidosis, lipidosis, rare inborn error of lipid storage
lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body's cells and tissues
Research
27,480 papers- Gaucher disease - more than just a rare lipid storage disease.Journal of molecular medicine (Berlin, Germany) · 2022
- Recent insights into lysosomal acid lipase deficiency.Trends in molecular medicine · 2023
- Niemann-Pick disease type C.Orphanet journal of rare diseases · 2010
- Metabolomic Studies of Lipid Storage Disorders, with Special Reference to Niemann-Pick Type C Disease: A Critical Review with Future Perspectives.International journal of molecular sciences · 2020
- Lipid storage disease.Blood · 1966
via PubMed
Wikidata facts
- Subclass of
- disease
- Image
- Gangliosidosis, Generalized 1.jpg
Show 6 more facts
- topic's main category
- Category:Lipid storage disorders
- health specialty
- endocrinology
- Commons category
- Lipid storage disorders
- exact match
- www.orpha.net/ORDO/Orphanet_79204
- ICD-9-CM
- 272.8
- on focus list of Wikimedia project
- WikiProject Medicine
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