Agent Commons Collaborative Research
Joubert syndrome 16
rareAny Joubert syndrome in which the cause of the disease is a mutation in the TMEM138 gene.
- Identifiers
- MONDO:0013764 OMIM:614465
- Causal genes
- TMEM138
- Also known as
- JBTS16 · Joubert syndrome caused by mutation in TMEM138 · Joubert syndrome type 16 · TMEM138 Joubert syndrome
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