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Summary Literature (0)
MIM:611523 - PONTOCEREBELLAR HYPOPLASIA, TYPE 6; PCH6

Xenbase Genes: rars2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012683 - pontocerebellar hypoplasia type 6

Disease Ontology (DO):
DOID:0060275 - pontocerebellar hypoplasia type 6