| CUI | Disease | Vocabulary | Name in Vocabulary | Code |
|---|---|---|---|---|
| C2700553 | Omenn Syndrome | DO | Omenn syndrome | 0060010 |
| C2700553 | Omenn Syndrome | EFO | histiocytic medullary reticulosis | 1001499 |
| C2700553 | Omenn Syndrome | MONDO | malignant histiocytosis | 0004612 |
| C2700553 | Omenn Syndrome | MONDO | Omenn syndrome | 0011338 |
| C2700553 | Omenn Syndrome | MSH | Severe Combined Immunodeficiency | D016511 |
| C2700553 | Omenn Syndrome | MSH | Bare Lymphocyte Syndrome | D016511 |
| C2700553 | Omenn Syndrome | MSH | Omenn Syndrome | D016511 |
| C2700553 | Omenn Syndrome | NCI | Omenn Syndrome | C61240 |
| C2700553 | Omenn Syndrome | OMIM | OMENN SYNDROME | 603554 |
| C2700553 | Omenn Syndrome | OMIM | RETICULOENDOTHELIOSIS, FAMILIAL, WITH EOSINOPHILIA | 603554 |
| C2700553 | Omenn Syndrome | ORDO | Omenn syndrome | 39041 |