Seckel Syndrome 8
Disease ID: disease_node_20372
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:615807 |
|---|---|
| Subclassof | DOID_0050569 |
| Data Source | DOID |
| Synonyms | SCKL8 |
| Doid Label | Seckel syndrome 8 |
| Doid Description | A Seckel syndrome that has_material_basis_in homozygous mutation in the DNA2 gene on chromosome 10q21. |
| Disease Node Id | disease_node_20372 |
| Doid Id | DOID_0070009 |
| Label | Seckel Syndrome 8 |
- Outgoing r'ship
SUBCLASS_OFto/from Seckel Syndrome(ID:disease_node_20368) (Disease)