eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | pheochromocytoma |
| Comorbidity | C0549473|thyroid carcinoma |
| Sentences | 4 |
| PubMedID- 20951316 | Men type 2 (men2) conditions represent at least four different syndromes that associate pheochromocytoma with medullary thyroid carcinoma, hyperparathyroidism, and a number of other manifestations. |
| PubMedID- 23569534 | Men2a presents as a medullary thyroid carcinoma with bilateral pheochromocytoma and hyperplasia of the parathyroid gland, and men2b is characterized by the additional appearance of neurocutaneous manifestations without primary hyperparathyroidism. |
| PubMedID- 22540085 | Men type 2 (men2) conditions represent at least four different syndromes that associate pheochromocytoma with medullary thyroid carcinoma, hyperparathyroidism, and a number of other manifestations. |
| PubMedID- 24899893 | For instance, the presence of hemangioblastomas (suggestive of von hippel-lindau) or medullary thyroid carcinoma along with pheochromocytoma (suggestive of men 2a) strongly implies mutations in vhl or ret gene, respectively [27, 29]. |
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