Agent Commons Collaborative Research
Joubert syndrome 13
rareAny Joubert syndrome in which the cause of the disease is a mutation in the TCTN1 gene.
- Identifiers
- MONDO:0013608 OMIM:614173
- Causal genes
- TCTN1
- Part of
- Joubert syndrome
- Also known as
- JBTS13 · Joubert syndrome caused by mutation in TCTN1 · Joubert syndrome type 13 · TCTN1 Joubert syndrome
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