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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


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