Meckel syndrome 1 (Q50349680)
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Meckel syndrome that has material basis in an autosomal recessive mutation of MKS1 on chromosome 17q22
- Meckel-Gruber syndrome, type 1
- MKS1
- Dysencephalia Splanchnocystica
- MKS
- Meckel syndrome type1
- Gruber Syndrome
- Dysencephalia splachnocystica
- Meckel-Gruber Syndrome
- Meckel Gruber syndrome
- Meckel Syndrome, Type 1
- Meckel Syndrome
- Meckel syndrome, type 1
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Meckel syndrome 1 |
Meckel syndrome that has material basis in an autosomal recessive mutation of MKS1 on chromosome 17q22 |
|
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Identifiers
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