Cowden Syndrome 4
Disease ID: disease_node_20172
Connections displayed (default: 10).
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| Dbxref | MIM:615107 |
|---|---|
| Subclassof | DOID_6457 |
| Data Source | DOID |
| Doid Label | Cowden syndrome 4 |
| Doid Description | A Cowden syndrome that has_material_basis_in heterozygous germline hypermethylation of the KLLN gene on chromosome 10q23. |
| Disease Node Id | disease_node_20172 |
| Doid Id | DOID_0081000 |
| Label | Cowden Syndrome 4 |
- Outgoing r'ship
SUBCLASS_OFto/from Hamartoma Syndrome, Multiple(ID:disease_node_3657) (Disease)