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Summary Literature (0)
MIM:615803 - PONTOCEREBELLAR HYPOPLASIA, TYPE 10; PCH10

Xenbase Genes: clp1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014349 - pontocerebellar hypoplasia type 10

Disease Ontology (DO):
DOID:0060279 - pontocerebellar hypoplasia type 10