Wolfram syndrome · Human disease · YYNN

Wolfram syndrome

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Human disease

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Wolfram syndrome 1

Subject of
5

Sleep disturbances in Wolfram syndrome

scientific article published on 02 August 2019

EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome

scientific article

Phenotypic characteristics of early Wolfram syndrome

scientific article published on April 27, 2013

Autosomal dominant diabetes arising from a Wolfram syndrome 1 mutation

scientific article published on 31 July 2013

Genotypic classification of patients with Wolfram syndrome: insights into the natural history of the disease and correlation with phenotype

scientific article published on February 21, 2013

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Wolfram syndrome, also called DIDMOAD (diabetes insipidus, diabetes mellitus, optic atrophy, and deafness), is a rare autosomal-recessive genetic disorder that causes childhood-onset diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders including neurodegeneration. Symptoms can start to appear as early as...

Instance of

designated intractable/rare disease

class of disease

Subclass of

Genetic disorder

Endocrine disease

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