Seckel syndrome 9 (Q50349578)
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Seckel syndrome that has material basis in homozygous mutation in the TRAIP gene on chromosome 3p21
- SCKL9
- Seckel Syndrome 9
- Seckel Syndrome type 9
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Seckel syndrome 9 |
Seckel syndrome that has material basis in homozygous mutation in the TRAIP gene on chromosome 3p21 |
|
Statements
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Identifiers
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