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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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Laminopathy
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Adult-onset autosomal dominant demyelinating leukodystrophy
Leukodystrophy, demyelinating, adult-onset, autosomal dominant, typical
rare
Identifiers
MONDO:0700295
OMIM:169500
Part of
Adult-onset autosomal dominant demyelinating leukodystrophy
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