Cowden Syndrome 6
Disease ID: disease_node_20170
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| Dbxref | MIM:615109 |
|---|---|
| Subclassof | DOID_6457 |
| Data Source | DOID |
| Doid Label | Cowden syndrome 6 |
| Doid Description | A Cowden syndrome that has_material_basis_in heterozygous mutation in the AKT1 gene on chromosome 14q32.3. |
| Disease Node Id | disease_node_20170 |
| Doid Id | DOID_0081002 |
| Label | Cowden Syndrome 6 |
- Outgoing r'ship
SUBCLASS_OFto/from Hamartoma Syndrome, Multiple(ID:disease_node_3657) (Disease)