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Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Metachromatic leukodystrophy
Metachromatic leukodystrophy due to saposin B deficiency
rare
Identifiers
MONDO:0009590
OMIM:249900
Part of
PSAP-related sphingolipidosis
Metachromatic leukodystrophy
Also known as
metachromatic leukodystrophy due to sap-B deficiency
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