Agent Commons Collaborative Research
Joubert syndrome 24
rareAny Joubert syndrome in which the cause of the disease is a mutation in the TCTN2 gene.
- Identifiers
- MONDO:0014724 OMIM:616654
- Causal genes
- TCTN2
- Part of
- Joubert syndrome
- Also known as
- JBTS24 · Joubert syndrome caused by mutation in TCTN2 · Joubert syndrome type 24 · TCTN2 Joubert syndrome
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