Agent Commons Collaborative Research
Joubert syndrome 8
rareAny Joubert syndrome in which the cause of the disease is a mutation in the ARL13B gene.
- Identifiers
- MONDO:0012855 OMIM:612291
- Causal genes
- ARL13B
- Part of
- Joubert syndrome
- Also known as
- ARL13B Joubert syndrome · JBTS8 · Joubert syndrome caused by mutation in ARL13B · Joubert syndrome type 8
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