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Summary Literature (0)
MIM:612389 - PONTOCEREBELLAR HYPOPLASIA, TYPE 2B; PCH2B

Xenbase Genes: tsen2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012890 - pontocerebellar hypoplasia type 2B
MONDO:0016759 - pontocerebellar hypoplasia type 2

Disease Ontology (DO):
DOID:0060268 - pontocerebellar hypoplasia type 2B