OBO ID: DOID:0110629 |
Term Name: | Wolfram syndrome 1 | Search Ontology: | |
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Definition: | An autosomal recessive disease that is characterized by diabetes mellitus, optic atrophy, and deafness as well as various other possible disorders and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the WFS1 gene on chromosome 4p16.1. https://www.ncbi.nlm.nih.gov/pubmed/21538838 | ||
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Ontology: | Human Disease ( DOID:0110629 ) |
OTHER Wolfram syndrome 1 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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