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MIM:614961 - PONTOCEREBELLAR HYPOPLASIA, TYPE 8; PCH8
Xenbase Genes: chmp1a
Human Disease Resource: MIM
MONDO:0013990 - pontocerebellar hypoplasia type 8 |
DOID:0060277 - pontocerebellar hypoplasia type 8 |
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MONDO:0013990 - pontocerebellar hypoplasia type 8 |
DOID:0060277 - pontocerebellar hypoplasia type 8 |