Cowden Syndrome 5
Disease ID: disease_node_20171
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| Dbxref | MIM:615108 |
|---|---|
| Subclassof | DOID_6457 |
| Data Source | DOID |
| Doid Label | Cowden syndrome 5 |
| Doid Description | A Cowden syndrome that has_material_basis_in heterozygous mutation in the PIK3CA gene on chromosome 3q26. |
| Disease Node Id | disease_node_20171 |
| Doid Id | DOID_0081001 |
| Label | Cowden Syndrome 5 |
- Outgoing r'ship
SUBCLASS_OFto/from Hamartoma Syndrome, Multiple(ID:disease_node_3657) (Disease)