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Krabbe's disease
Used for:
beta galactocerebrosidase deficiency
Used for:
galactosylceramide lipidosis
Used for:
globoid cell leukodystrophy
Used for:
Krabbe's leukodystrophy
Broader Terms:
enzyme deficiency
Broader Terms:
inborn lysosomal enzyme disorder
Broader Terms:
leukodystrophy
Scope Note:
inherited, demyelinating, human lipid storage disease caused by a deficiency of galactosylceramidase; manifestations include convulsions, quadriplegia, blindness, deafness, and mental retardation.
Term Number:
1849-5536
Send your comments to: Melody Lowe