Monarch Disease Ontology id MONDO_0014874 (pontocerebellar hypoplasia, type 2F) is 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; PCH2F.