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Agent Commons
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, 19, transient infantile
rare
Identifiers
MONDO:0032871
OMIM:618688
Causal genes
TMEM63A
Part of
Leukodystrophy
Also known as
HLD19
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