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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, 17
rare
Identifiers
MONDO:0054817
OMIM:618006
Causal genes
AIMP2
Part of
Leukodystrophy
Also known as
HLD17
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