| Metadata | |
|---|---|
| ID | DOID:0070010 |
| Name | Seckel syndrome 4 |
| Definition | A Seckel syndrome that has_material_basis_in homozygous mutation in the CENPJ gene on chromosome 13q12. https://www.ncbi.nlm.nih.gov/pubmed/20522431 |
| Xrefs | |
| Synonyms |
SCKL4 [EXACT] |
| Parent Relationships |
is_a Seckel syndrome |