eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | pheochromocytoma |
| Comorbidity | C0221002|primary hyperparathyroidism |
| Sentences | 2 |
| PubMedID- 23776920 | primary hyperparathyroidism (php) with pheochromocytoma and neurofibromatosis type 1 is a rare clinical association. |
| PubMedID- 24394853 | Hereditary mtc can manifest either alone as familial mtc or as part of the multiple endocrine neoplasia type 2 syndromes (men 2).4 men 2 involves medullary carcinoma and pheochromocytoma with either primary hyperparathyroidism (men 2a) or marfanoid habitus and mucosal neurofibromatosis (men 2b). |
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