|
MIM:612359 - MOVED TO 158350
Xenbase Genes:
Human Disease Resource: MIM
| MONDO:0012878 - Cowden syndrome 2 |
| MONDO:0016063 - Cowden disease |
| DOID:6457 - Cowden syndrome |
|
| MONDO:0012878 - Cowden syndrome 2 |
| MONDO:0016063 - Cowden disease |
| DOID:6457 - Cowden syndrome |