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Pontocerebellar hypoplasia type 10
rareAny non-syndromic pontocerebellar hypoplasia in which the cause of the disease is a mutation in the CLP1 gene.
- Identifiers
- MONDO:0014349 OMIM:615803Orphanet:411493
- Causal genes
- CLP1
- Part of
- Pontocerebellar hypoplasia
- Also known as
- CLP1 non-syndromic pontocerebellar hypoplasia · CLP1-related pontocerebellar hypoplasia · non-syndromic pontocerebellar hypoplasia caused by mutation in CLP1 · PCH10 · pontocerebellar hypoplasia, type 10
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