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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
/
Inherited neurodegenerative disorder
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Leukodystrophy
Leukodystrophy, hypomyelinating, 14
rare
Identifiers
MONDO:0033486
OMIM:617899
Causal genes
UFM1
Part of
Leukodystrophy
Also known as
HLD14
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