Pontocerebellar hypoplasia type 10

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.