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Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Inherited neurodegenerative disorder
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Leukodystrophy
Leukodystrophy, hypomyelinating, 26, with chondrodysplasia
rare
Identifiers
MONDO:0859518
OMIM:620269
Causal genes
SLC35B2
Part of
Leukodystrophy
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