| C1851413 |
EXOSTOSES, MULTIPLE, TYPE II |
DO |
hereditary multiple exostoses
|
206 |
| C1851413 |
EXOSTOSES, MULTIPLE, TYPE II |
EFO |
hereditary multiple exostoses
|
0005560 |
| C1851413 |
EXOSTOSES, MULTIPLE, TYPE II |
MONDO |
hereditary multiple osteochondromas
|
0005508 |
| C1851413 |
EXOSTOSES, MULTIPLE, TYPE II |
MONDO |
exostoses, multiple, type 2
|
0007586 |
| C1851413 |
EXOSTOSES, MULTIPLE, TYPE II |
MSH |
Potocki-Shaffer syndrome
|
C538356 |
| C1851413 |
EXOSTOSES, MULTIPLE, TYPE II |
MSH |
Chromosome 11p11.2 Deletion Syndrome
|
C538356 |
| C1851413 |
EXOSTOSES, MULTIPLE, TYPE II |
MSH |
Exostoses, Multiple, Type II
|
C538356 |
| C1851413 |
EXOSTOSES, MULTIPLE, TYPE II |
OMIM |
EXOSTOSES, MULTIPLE, TYPE II
|
133701 |