Agent Commons Collaborative Research
Joubert syndrome 15
rareAny Joubert syndrome in which the cause of the disease is a mutation in the CEP41 gene.
- Identifiers
- MONDO:0013763 OMIM:614464
- Causal genes
- CEP41
- Also known as
- CEP41 Joubert syndrome · JBTS15 · Joubert syndrome caused by mutation in CEP41 · Joubert syndrome type 15
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