Meckel syndrome 6 (Q50349685)
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A Meckel syndrome that has material basis in an autosomal recessive mutation of CC2D2A on chromosome 4p15.32.
- MKS6
- Meckel-Gruber syndrome, type 6
- MECKEL SYNDROME, TYPE 6
- MECKEL SYNDROME, TYPE 6; MKS6
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Meckel syndrome 6 |
A Meckel syndrome that has material basis in an autosomal recessive mutation of CC2D2A on chromosome 4p15.32. |
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Statements
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