Pontocerebellar hypoplasia, type 2F

Any non-syndromic pontocerebellar hypoplasia in which the cause of the disease is a mutation in the TSEN15 gene.

Also known as: PCH2F, TSEN15 non-syndromic pontocerebellar hypoplasia, non-syndromic pontocerebellar hypoplasia caused by mutation in TSEN15, pontocerebellar hypoplasia, type 2F, pontocerebellar hypoplasia, type 2F; PCH2F

10 clinical trials for this condition and its sub-types.