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Human Disease

autosomal dominant Wolfram syndrome

Term ID
DOID:0080584
Synonyms
Definition
A Wolfram syndrome that is characterized by congenital progressive hearing impairment, diabetes mellitus, and optic atrophy and that has_material_basis_in autosomal dominant inheritance of a heterozygous mutation in the WFS1 gene on chromosome 4p16. https://www.ncbi.nlm.nih.gov/pubmed/18544103
References
Ontology
Human Disease   ( DOID:0080584 )
Relationships
is a type of
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Genes Involved
Zebrafish Models