| Metadata | |
|---|---|
| ID | DOID:0070011 |
| Name | Seckel syndrome 7 |
| Definition | A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NIN gene on chromosome 14q22. https://www.ncbi.nlm.nih.gov/pubmed/22933543 |
| Xrefs | |
| Synonyms |
SCKL7 [EXACT] |
| Parent Relationships |
is_a Seckel syndrome |