eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| Disease | hyperparathyroidism |
| Comorbidity | C0031511|pheochromocytoma |
| Sentences | 3 |
| 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). |
| PubMedID- 24449023 | Multiple endocrine neoplasia type 2 (men2) is an autosomal, dominantly inherited disorder manifesting various combinations of medullary thyroid carcinoma (mtc) and pheochromocytoma, with hyperparathyroidism (men2a) or neuromas of the enteric autonomic nerve cells (men2b). |
| PubMedID- 23776920 | Primary hyperparathyroidism (php) with pheochromocytoma and neurofibromatosis type 1 is a rare clinical association. |
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