MeSH Browser

MeSH Supplementary: Islet cell tumor syndrome
Unique ID: C531777
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C531777
Entry Term(s): Bilateral pheochromocytoma and islet cell adenoma of the pancreas; Chromaffinoma; Familial islet cell tumors; Familial pheochromocytoma
Registry Number: 0
Heading Mapped to: *Pancreatic Neoplasms; *Pheochromocytoma
Frequency: 21
Note: Hereditary PHEOCHROMOCYTOMA that originates in ISLET CELLS. Affected individuals have systemic symptoms that may include cerebral hemorrhage, episodic hypertension, sweating, TACHYCARDIA; HYPERTENSIVE RETINOPATHY; CAFÉ-AU-LAIT SPOTS; and excess NOREPINEPHRINE in urine. OMIM: 171420
Date of Entry: 2010/08/25
Revision Date: 2020/09/30

Islet cell tumor syndrome MeSH Supplementary Concept Data 2024