Meckel syndrome type 7 (Q3508640)
(Redirected from Q50349687)
A Meckel syndrome that has material basis in an autosomal recessive mutation of NPHP3 on chromosome 3q22.1.
- Goldston syndrome
- Meckel syndrome 7
- Meckel-Gruber syndrome, type 7
- MKS7
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Meckel syndrome type 7 |
A Meckel syndrome that has material basis in an autosomal recessive mutation of NPHP3 on chromosome 3q22.1. |
|
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Identifiers
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Sitelinks
Wikipedia(1 entry)
- frwiki Syndrome de Goldston