eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | multiple endocrine neoplasia |
| Symptom | C0796095|c syndrome |
| Sentences | 2 |
| PubMedID- 22261919 | Specific points related to gastrinomas associated with the genetic syndrome of multiple endocrine neoplasia type 1 (men1) (25% of cases) will also be mentioned . |
| 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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