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[Wolfram syndrome]. 1986

N S Mazalova, and N B Kovaleva

UI MeSH Term Description Entries
D008297 Male Males
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D014929 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. DIDMOAD,DIDMOAD Syndrome,DIDMOADUD,Diabetes Insipidus and Mellitus with Optic Atrophy and Deafness,Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness,Wolfram Syndrome 1,Syndrome, Wolfram

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