Cowden Syndrome 7
Disease ID: disease_node_20169
Connections displayed (default: 10).
Loading graph...
| Dbxref | MIM:616858 |
|---|---|
| Subclassof | DOID_6457 |
| Data Source | DOID |
| Doid Label | Cowden syndrome 7 |
| Doid Description | A Cowden syndrome that has_material_basis_in heterozygous mutation in the SEC23B gene on chromosome 20p11. |
| Disease Node Id | disease_node_20169 |
| Doid Id | DOID_0081003 |
| Label | Cowden Syndrome 7 |
- Outgoing r'ship
SUBCLASS_OFto/from Hamartoma Syndrome, Multiple(ID:disease_node_3657) (Disease)