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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, 22
rare
Identifiers
MONDO:0025701
OMIM:619328
Causal genes
CLDN11
Part of
Leukodystrophy
Also known as
HLD22
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