PedAM
Pediatric Disease Annotations & Medicines
| Disease | c syndrome |
| Phenotype | C0027662|multiple endocrine neoplasia |
| Sentences | 2 |
| 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). |
| PubMedID- 24678435 | Genetic syndromes associated with icts include multiple endocrine neoplasia type 1, von hippel-lindau disease, von recklinghausen disease, and tuberous sclerosis. |
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