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bn:00707777n
Noun Concept
Categories: Autosomal recessive disorders, Rare diseases, Demyelinating diseases of CNS, Neurological disorders in children, Diseases named for discoverer
EN
Krabbe disease  Galactosylceramide beta-galactosidase deficiency  beta galactocerebrosidase deficiency  diffuse globoid body sclerosis  Galactocerebrosidase deficiency
EN
Krabbe disease is a rare and often fatal lysosomal storage disease that results in progressive damage to the nervous system. Wikipedia
Definitions
Relations
Sources
EN
Krabbe disease is a rare and often fatal lysosomal storage disease that results in progressive damage to the nervous system. Wikipedia
Krabbe disease is a lysosomal disorder that affects the white matter of the central and peripheral nervous systems. It includes infantile, late-infantile/juvenile and adult forms. Wikidata
IS A
rare disease
sphingolipidosis
GENETIC ASSOCIATION
prosaposin
galactosylceramidase
HEALTH SPECIALTY
metabolic disorder
NAMED AFTER
Knud Krabbe
Wikipedia
EN
Krabbe disease
Wikidata
EN
Krabbe disease
Wikipedia Redirections
EN
Diffuse Globoid Body Sclerosis, Galactosyl ceramide lipidosis, galactosylceramide lipidosis, Gfalactosyl ceramide lipidosis, globoid cell leukodystrophy, Krabbe's disease, Krabbe Disease, Krabbe leukodystrophy, Krabbes disease, Krabbé disease, Leukodystrophy, globoid cell
Wikidata Alias
EN
beta galactocerebrosidase deficiency, diffuse globoid body sclerosis, Galactocerebrosidase deficiency, Galactosylceramidase deficiency, Galactosylceramide beta-galactosidase deficiency, Galactosylceramide Lipidosis, Galc Deficiency, globoid cell leukodystrophy, globoid cell leukoencephalopathy, Krabbe's disease, Krabbe's leukodystrophy, KRABBE DISEASE

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