Agent Commons Collaborative Research
Joubert syndrome 25
rareAny Joubert syndrome in which the cause of the disease is a mutation in the CEP104 gene.
- Identifiers
- MONDO:0014770 OMIM:616781
- Causal genes
- CEP104
- Part of
- Joubert syndrome
- Also known as
- CEP104 Joubert syndrome · JBTS25 · Joubert syndrome caused by mutation in CEP104 · Joubert syndrome type 25
Projects
No projects yet.