| CUI | Disease | Vocabulary | Name in Vocabulary | Code |
|---|---|---|---|---|
| C0013366 | Dyschondroplasias | DO | hereditary multiple exostoses | 206 |
| C0013366 | Dyschondroplasias | DO | Ollier disease | 4624 |
| C0013366 | Dyschondroplasias | MONDO | Ollier disease | 0008145 |
| C0013366 | Dyschondroplasias | MSH | Dyschondroplasias | D010009 |
| C0013366 | Dyschondroplasias | MSH | Melnick-Needles Syndrome | D010009 |
| C0013366 | Dyschondroplasias | MSH | Multiple Epiphyseal Dysplasia | D010009 |
| C0013366 | Dyschondroplasias | MSH | Osteochondrodysplasias | D010009 |
| C0013366 | Dyschondroplasias | MSH | Schwartz-Jampel Syndrome | D010009 |
| C0013366 | Dyschondroplasias | MSH | Spondyloepiphyseal Dysplasia | D010009 |
| C0013366 | Dyschondroplasias | MSH | Van Buchem Disease | D010009 |
| C0013366 | Dyschondroplasias | MSH | Spondyloepiphyseal Dysplasia Tarda, X-Linked | D010009 |
| C0013366 | Dyschondroplasias | MSH | Schwartz-Jampel Syndrome, Type 1 | D010009 |
| C0013366 | Dyschondroplasias | ORDO | Ollier disease | 296 |