Krabbe disease

rare

A lysosomal disorder that affects the white matter of the central and peripheral nervous systems. It includes infantile, late-infantile/juvenile and adult forms.

Identifiers: MONDO:0009499 OMIM:245200 Orphanet:487
Causal genes: GALC
Part of: Eye degenerative disorder Hereditary peripheral neuropathy Leukodystrophy Sphingolipidosis
Also known as: diffuse globoid body sclerosis · galactocerebrosidase deficiency · galactosylceramidase deficiency · galactosylceramide lipidosis · GALC deficiency

Subtypes

All diseases Rare only

Disease	ID	Subtypes
Adult Krabbe disease	MONDO:0016091
Infantile Krabbe disease	MONDO:0016089
Late-infantile/juvenile Krabbe disease	MONDO:0016090

Rare disease

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