| Metadata | |
|---|---|
| ID | DOID:0070009 |
| Name | Seckel syndrome 8 |
| Definition | A Seckel syndrome that has_material_basis_in homozygous mutation in the DNA2 gene on chromosome 10q21. https://www.ncbi.nlm.nih.gov/pubmed/24389050 |
| Xrefs | |
| Synonyms |
SCKL8 [EXACT] |
| Parent Relationships |
is_a Seckel syndrome |