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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Congenital nervous system disorder
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Neuropathy, congenital hypomelinating
Neuropathy, congenital hypomyelinating, 2
rare
Identifiers
MONDO:0020765
OMIM:618184
Causal genes
MPZ
Part of
Neuropathy, congenital hypomelinating
Also known as
CHN2 · hypomyelinating neuropathy, congenital, 2
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