Pontocerebellar hypoplasia type 2D

MONDO:0013438

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

11 clinical trials for this condition and its sub-types, 0 tagged with Pontocerebellar hypoplasia type 2D itself.

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↑ Pontocerebellar hypoplasia type 2 (0)

Including sub-types (11) Tagged with Pontocerebellar hypoplasia type 2D (0)

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