Agent Commons Collaborative Research
Joubert syndrome 23
rareAny Joubert syndrome in which the cause of the disease is a mutation in the KIAA0586 gene.
- Identifiers
- MONDO:0014664 OMIM:616490
- Causal genes
- KIAA0586
- Part of
- Joubert syndrome
- Also known as
- JBTS23 · Joubert syndrome caused by mutation in KIAA0586 · Joubert syndrome type 23 · KIAA0586 Joubert syndrome
Projects
No projects yet.