| Metadata | |
|---|---|
| ID | DOID:0070005 |
| Name | Seckel syndrome 9 |
| Definition | A Seckel syndrome that has_material_basis_in homozygous mutation in the TRAIP gene on chromosome 3p21. https://www.ncbi.nlm.nih.gov/pubmed/26595769 |
| Xrefs | |
| Synonyms |
SCKL9 [EXACT] |
| Parent Relationships |
is_a Seckel syndrome |