Seckel Syndrome 7
Disease ID: disease_node_20370
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:614851 |
|---|---|
| Subclassof | DOID_0050569 |
| Data Source | DOID |
| Synonyms | SCKL7 |
| Doid Label | Seckel syndrome 7 |
| Doid Description | A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NIN gene on chromosome 14q22. |
| Disease Node Id | disease_node_20370 |
| Doid Id | DOID_0070011 |
| Label | Seckel Syndrome 7 |
- Outgoing r'ship
SUBCLASS_OFto/from Seckel Syndrome(ID:disease_node_20368) (Disease)