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bn:00037508n
Noun Concept
Categories: Lipid storage disorders, Skin conditions resulting from errors in metabolism, Diseases named for discoverer, Rare diseases, Articles with permanently dead external links
EN
Gaucher's disease  Gauchers disease  lipoid histiocytosis  National Gaucher Foundation  acid beta-glucosidase deficiency
EN
A rare chronic disorder of lipid metabolism of genetic origin WordNet 3.0
Definitions
Relations
Sources
EN
A rare chronic disorder of lipid metabolism of genetic origin WordNet 3.0 & Open English WordNet
Gaucher's disease or Gaucher disease is a genetic disorder in which glucocerebroside accumulates in cells and certain organs. Wikipedia
A lipid storage diseases Wikipedia Disambiguation
Human disease characterized by deficiency of the enzyme glucocerebrosidase which results in the accumulation of harmful quantities of the glycolipid glucocerebroside throughout the body Wikidata
A genetic disease in which lipid accumulates in cells and certain organs. Wiktionary
Genetic disease in which lipid accumulates in cells and certain organs. Wiktionary (translation)
IS A
lipidosis
monogenic disorder
rare disease
sphingolipidosis
DRUG USED FOR TREATMENT
cycloserine
miglustat
Velaglucerase alfa
imiglucerase
eliglustat
GENETIC ASSOCIATION
prosaposin
glucocerebrosidase
NTRK3
HEALTH SPECIALTY
neurology
endocrinology
NAMED AFTER
Philippe Gaucher
WordNet 3.0 & Open English WordNet
EN
Gaucher's disease
Wikipedia
EN
Gaucher's disease
Wikidata
EN
Gaucher's disease
Wiktionary
EN
Gaucher's disease
Wikipedia Redirections
EN
Acid beta-glucosidase deficiency, Acute cerebral Gaucher's disease, Anemia, splenic, familial, Cerebroside Lipidosis syndrome, Epidemiology of N370S in the United States, Erlenmeyer flask deformity of the femur, Gaucher's, Gaucher's Disease, Gaucher's disease epidemiology in USA, Gaucher disease, Gaucher disease type 1, Gaucher disease type 2, Gaucher disease type 3, Gaucher syndrome, Gauchers disease, Gauchers Disease, Gaucher’s disease, N370S in the United States, National Gaucher Foundation, Prevalence of N370S in the United States, Pseudo-Gaucher disease
Wikidata Alias
EN
acid beta-glucosidase deficiency, Gaucher disease, glocucerebrosidase deficiency, Glucocerebrosidase deficiency, glucosylceramide beta-glucosidase deficiency, kerasin thesaurismosis, lipoid histiocytosis

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