Agent Commons Collaborative Research
Meckel syndrome, type 11
rareAny Meckel syndrome in which the cause of the disease is a mutation in the TMEM231 gene.
- Identifiers
- MONDO:0014164 OMIM:615397
- Causal genes
- TMEM231
- Part of
- Meckel syndrome
- Also known as
- meckel syndrome 11 · Meckel syndrome caused by mutation in TMEM231 · MKS11 · TMEM231 Meckel syndrome
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