OBO ID: DOID:0080584 |
Term Name: | autosomal dominant Wolfram syndrome | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0080584 ) |
OTHER autosomal dominant Wolfram syndrome PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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