| Metadata | |
|---|---|
| ID | DOID:0070012 |
| Name | Seckel syndrome 5 |
| Definition | A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21. https://www.ncbi.nlm.nih.gov/pubmed/21131973 |
| Xrefs | |
| Synonyms |
SCKL5 [EXACT] |
| Parent Relationships |
is_a Seckel syndrome |