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Summary Literature (0)
MIM:614678 - PONTOCEREBELLAR HYPOPLASIA, TYPE 1B; PCH1B

Xenbase Genes: exosc3

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013853 - pontocerebellar hypoplasia type 1B
MONDO:0016396 - pontocerebellar hypoplasia type 1

Disease Ontology (DO):
DOID:0060266 - pontocerebellar hypoplasia type 1B