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Summary Literature (0)
MIM:615809 - PONTOCEREBELLAR HYPOPLASIA, TYPE 9; PCH9

Xenbase Genes: ampd2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014351 - pontocerebellar hypoplasia type 9

Disease Ontology (DO):
DOID:0060278 - pontocerebellar hypoplasia type 9