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Summary Literature (0)
MIM:617695 - PONTOCEREBELLAR HYPOPLASIA, TYPE 11; PCH11

Xenbase Genes: tbc1d23

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0054669 - pontocerebellar hypoplasia, type 11

Disease Ontology (DO):
DOID:0112324 - pontocerebellar hypoplasia type 11