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Summary Literature (0)
MIM:607596 - PONTOCEREBELLAR HYPOPLASIA, TYPE 1A; PCH1A

Xenbase Genes: vrk1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011866 - pontocerebellar hypoplasia type 1A
MONDO:0016396 - pontocerebellar hypoplasia type 1

Disease Ontology (DO):
DOID:0060265 - pontocerebellar hypoplasia type 1A