Disease | pheochromocytoma |
Symptom | C0426576|gastrointestinal symptoms |
Sentences | 1 |
PubMedID- 22429913 | Multiple endocrine neoplasia type 2 b (men 2b) is a rare autosomal dominant complex neoplastic neurocristopathy characterized by the development of a number of tumors including medullary thyroid carcinoma (mtc) and pheochromocytoma (pheo) with gastrointestinal symptoms, marphanoid facies and multiple ganglioneuromas (gn)/ganglioneurofibromas(gnf) 1. |
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