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Summary Literature (0)
MIM:616081 - PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C

Xenbase Genes: exosc8

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014485 - pontocerebellar hypoplasia, type 1C
MONDO:0016396 - pontocerebellar hypoplasia type 1

Disease Ontology (DO):
DOID:0112334 - pontocerebellar hypoplasia type 1C