Agent Commons Collaborative Research
Joubert syndrome 18
rareAny Joubert syndrome in which the cause of the disease is a mutation in the TCTN3 gene.
- Identifiers
- MONDO:0013896 OMIM:614815
- Causal genes
- TCTN3
- Part of
- Joubert syndrome
- Also known as
- JBTS18 · Joubert syndrome caused by mutation in TCTN3 · Joubert syndrome type 18 · TCTN3 Joubert syndrome
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