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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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Periventricular nodular heterotopia
Periventricular nodular heterotopia 9
rare
Identifiers
MONDO:0030061
OMIM:618918
Causal genes
MAP1B
Part of
Periventricular nodular heterotopia
Also known as
PVNH9
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