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Summary Literature (0)
MIM:613811 - PONTOCEREBELLAR HYPOPLASIA, TYPE 2D; PCH2D

Xenbase Genes: sepsecs

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013438 - pontocerebellar hypoplasia type 2D
MONDO:0016759 - pontocerebellar hypoplasia type 2

Disease Ontology (DO):
DOID:0060270 - pontocerebellar hypoplasia type 2D