Seckel syndrome 5 (Q50349585)
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Seckel syndrome that has material basis in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21
- SCKL5
- SECKEL SYNDROME 5
- SECKEL SYNDROME 5; SCKL5
- Seckel Syndrome type 5
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Seckel syndrome 5 |
Seckel syndrome that has material basis in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21 |
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