PedAM
Pediatric Disease Annotations & Medicines
| Disease | omenn syndrome |
| Phenotype | C0085110|severe combined immunodeficiency syndrome |
| Sentences | 1 |
| PubMedID- 23163657 | Accordingly, artemis mutations can lead to omenn syndrome, which is associated with human radiosensitive severe combined immunodeficiency syndrome and alopecia. |
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