Meckel syndrome 2 (Q50349681)
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A Meckel syndrome that has material basis in an autosomal recessive mutation of TMEM216 on chromosome 11q12.2.
- MKS2
- Meckel-Gruber syndrome, type 2
- MECKEL SYNDROME, TYPE 2; MKS2
- Meckel syndrome type 2
- MECKEL SYNDROME, TYPE 2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Meckel syndrome 2 |
A Meckel syndrome that has material basis in an autosomal recessive mutation of TMEM216 on chromosome 11q12.2. |
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