Pontocerebellar hypoplasia type 10

MONDO:0014349

Any non-syndromic pontocerebellar hypoplasia in which the cause of the disease is a mutation in the CLP1 gene.

Also known as: CLP1 non-syndromic pontocerebellar hypoplasia, CLP1-related pontocerebellar hypoplasia, PCH10, non-syndromic pontocerebellar hypoplasia caused by mutation in CLP1, pontocerebellar hypoplasia, type 10

1 clinical trial for this condition and its sub-types, 0 tagged with Pontocerebellar hypoplasia type 10 itself.

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↑ Pontocerebellar hypoplasia (3)

Including sub-types (1) Tagged with Pontocerebellar hypoplasia type 10 (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.