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Summary Literature (0)
MIM:608027 - PONTOCEREBELLAR HYPOPLASIA, TYPE 3; PCH3

Xenbase Genes: pclo

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011948 - pontocerebellar hypoplasia type 3

Disease Ontology (DO):
DOID:0060272 - pontocerebellar hypoplasia type 3