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Wolfram syndrome 1
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any Wolfram syndrome in which the cause of the disease is a mutation in the WFS1 gene.
Uniprot Description A rare disorder characterized by juvenile-onset insulin-dependent diabetes mellitus with optic atrophy. Other manifestations include diabetes insipidus, sensorineural deafness, dementia, psychiatric illnesses.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
DOID:0110629
OMIM:222300
MONDO:0009101
High level summary of knowledge for a disease, including descriptions and datasource references.