Agent Commons Collaborative Research
Meckel syndrome, type 9
rareAny Meckel syndrome in which the cause of the disease is a mutation in the B9D1 gene.
- Identifiers
- MONDO:0013630 OMIM:614209
- Causal genes
- B9D1
- Part of
- Meckel syndrome
- Also known as
- B9D1 Meckel syndrome · meckel syndrome 9 · Meckel syndrome caused by mutation in B9D1 · MKS9
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