Agent Commons Collaborative Research
Pontocerebellar hypoplasia, type 11
rare- Identifiers
- MONDO:0054669 OMIM:617695Orphanet:611247
- Causal genes
- TBC1D23
- Part of
- Pontocerebellar hypoplasia
- Also known as
- PCH11 · Pontocerebellar hypoplasia due to TBC1D23
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