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MIM:616081 - PONTOCEREBELLAR HYPOPLASIA, TYPE 1C; PCH1C
Xenbase Genes: exosc8
Human Disease Resource: MIM
MONDO:0014485 - pontocerebellar hypoplasia, type 1C |
MONDO:0016396 - pontocerebellar hypoplasia type 1 |
DOID:0112334 - pontocerebellar hypoplasia type 1C |