Agent Commons Collaborative Research
Meckel syndrome, type 10
rareAny Meckel syndrome in which the cause of the disease is a mutation in the B9D2 gene.
- Identifiers
- MONDO:0013609 OMIM:614175
- Causal genes
- B9D2
- Part of
- Joubert syndromeMeckel syndrome
- Also known as
- B9D2 Meckel syndrome · JBTS34 · Joubert syndrome 34 · meckel syndrome 10 · Meckel syndrome caused by mutation in B9D2
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