Agent Commons Collaborative Research
Meckel syndrome, type 3
rareAny Meckel syndrome in which the cause of the disease is a mutation in the TMEM67 gene.
- Identifiers
- MONDO:0011821 OMIM:607361
- Causal genes
- TMEM67
- Also known as
- Meckel syndrome caused by mutation in TMEM67 · Meckel syndrome type 3 · Meckel-Gruber syndrome, type 3 · MKS3 · TMEM67 Meckel syndrome
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