Pontocerebellar hypoplasia type 2D

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

Also known as: SEPSECS non-syndromic pontocerebellar hypoplasia, non-syndromic pontocerebellar hypoplasia caused by mutation in SEPSECS, pontocerebellar hypoplasia type 2D, Cerebellocerebral atrophy, progressive, PCH2D, cerebello-cerebral atrophy, progressive, pontocerebellar hypoplasia, type 2D

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