|
MIM:612359 - MOVED TO 158350
Xenbase Genes:
Human Disease Resource: OMIM
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 |