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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Central nervous system malformation
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Pontocerebellar hypoplasia
Pontocerebellar hypoplasia, type 13
rare
Identifiers
MONDO:0032831
OMIM:618606
Orphanet:613267
Causal genes
VPS51
Part of
Pontocerebellar hypoplasia
Also known as
PCH13
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