Definitions of wolfram syndrome

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Definition of 'wolfram syndrome'

U.S. National Library of Medicine

1. wolfram syndrome
A hereditary condition characterized by multiple symptoms including those of DIABETES INSIPIDUS; DIABETES MELLITUS; OPTIC ATROPHY; and DEAFNESS. This syndrome is also known as DIDMOAD (first letter of each word) and is usually associated with VASOPRESSIN deficiency. It is caused by mutations in gene WFS1 encoding wolframin, a 100-kDa transmembrane protein.

'wolfram syndrome' - Nearby Entries
wolf-hirschhorn syndrome wolff-parkinson-white syndrome wolffian ducts wolfram syndrome wolinella wolman disease women's health

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