Seckel syndrome 2 (Q50349586)
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Seckel syndrome that has material basis in homozygous mutation in the RBBP8 gene on chromosome 18q11
- Seckel-type dwarfism 2
- microcephalic primordial dwarfism 2
- SCKL2
- SECKEL SYNDROME 2; SCKL2
- SECKEL SYNDROME 2
- Seckel Syndrome type 2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Seckel syndrome 2 |
Seckel syndrome that has material basis in homozygous mutation in the RBBP8 gene on chromosome 18q11 |
|
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