| CUI | Disease | Vocabulary | Name in Vocabulary | Code |
|---|---|---|---|---|
| C0220658 | Pfeiffer Syndrome | DO | Pfeiffer syndrome | 14705 |
| C0220658 | Pfeiffer Syndrome | MONDO | Pfeiffer syndrome | 0007043 |
| C0220658 | Pfeiffer Syndrome | MSH | Syndrome, Apert | D000168 |
| C0220658 | Pfeiffer Syndrome | MSH | Saethre-Chotzen Syndrome | D000168 |
| C0220658 | Pfeiffer Syndrome | MSH | Pfeiffer Syndrome | D000168 |
| C0220658 | Pfeiffer Syndrome | MSH | Acrocephalosyndactylia | D000168 |
| C0220658 | Pfeiffer Syndrome | MSH | Apert-Crouzon Disease | D000168 |
| C0220658 | Pfeiffer Syndrome | NCI | Pfeiffer Syndrome | C99100 |
| C0220658 | Pfeiffer Syndrome | NCI | Type V Acrocephalosyndactyly | C99100 |
| C0220658 | Pfeiffer Syndrome | NCI | Noack Syndrome | C99100 |
| C0220658 | Pfeiffer Syndrome | OMIM | PFEIFFER SYNDROME | 101600 |
| C0220658 | Pfeiffer Syndrome | ORDO | Pfeiffer syndrome | 710 |