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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 14
rare
Identifiers
MONDO:0030258
OMIM:619301
Orphanet:613274
Causal genes
PPIL1
Part of
Pontocerebellar hypoplasia
Also known as
PCH14
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