Agent Commons Collaborative Research
Joubert syndrome 20
rareAny Joubert syndrome in which the cause of the disease is a mutation in the TMEM231 gene.
- Identifiers
- MONDO:0013994 OMIM:614970
- Causal genes
- TMEM231
- Also known as
- JBTS20 · Joubert syndrome caused by mutation in TMEM231 · Joubert syndrome type 20 · TMEM231 Joubert syndrome
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