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Summary Literature (0)
MIM:614961 - PONTOCEREBELLAR HYPOPLASIA, TYPE 8; PCH8

Xenbase Genes: chmp1a

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013990 - pontocerebellar hypoplasia type 8

Disease Ontology (DO):
DOID:0060277 - pontocerebellar hypoplasia type 8