| Metadata | |
|---|---|
| ID | DOID:0070006 |
| Name | Seckel syndrome 6 |
| Definition | A Seckel syndrome that has_material_basis_in homozygous mutation in the CEP63 gene on chromosome 3q22. https://www.ncbi.nlm.nih.gov/pubmed/21983783 |
| Xrefs | |
| Synonyms |
SCKL6 [EXACT] |
| Parent Relationships |
is_a Seckel syndrome |