MONDO_0014349 (pontocerebellar hypoplasia type 10) is 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.