A hereditary condition characterized by multiple symptoms including those of ; ; ; and . This syndrome is also known as DIDMOAD (first letter of each word) and is usually associated with deficiency. It is caused by mutations in gene WFS1 encoding wolframin, a 100-kDa transmembrane protein.
DIDMOAD Syndrome /
Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness /
Syndrome, Wolfram /