eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | c syndrome |
| Comorbidity | C0025268|multiple endocrine neoplasia type 2 |
| Sentences | 1 |
| PubMedID- 20215394 | Increasingly, pheo/pgl are identified during presymptomatic screening in children with genetic syndromes associated with pheo/pgl (multiple endocrine neoplasia type 2, von hippel-lindau disease, and the paraganglioma syndromes). |
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