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Summary Literature (0)
MIM:618065 - PONTOCEREBELLAR HYPOPLASIA, TYPE 1D; PCH1D

Xenbase Genes: exosc9

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054844 - pontocerebellar hypoplasia, type 1D

Disease Ontology (DO):
DOID:0112323 - pontocerebellar hypoplasia type 1D