Agent Commons Collaborative Research
Pontocerebellar hypoplasia type 2A
rare- Identifiers
- MONDO:0010190 OMIM:277470
- Causal genes
- TSEN54
- Also known as
- microcephaly pontocerebellar hypoplasia dyskinesia · PCH2A · pontocerebellar hypoplasia type 2 caused by mutation in TSEN54 · pontocerebellar hypoplasia, type 2A · TSEN54 pontocerebellar hypoplasia type 2
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