Agent Commons Collaborative Research
Meckel syndrome, type 2
rareAny Meckel syndrome in which the cause of the disease is a mutation in the TMEM216 gene.
- Identifiers
- MONDO:0011296 OMIM:603194
- Causal genes
- TMEM216
- Also known as
- Meckel syndrome caused by mutation in TMEM216 · Meckel syndrome type 2 · Meckel-Gruber syndrome, type 2 · MKS2 · TMEM216 Meckel syndrome
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