|OBO ID: DOID:0110490|
|Term Name:||autosomal recessive nonsyndromic deafness 31||Search Ontology:|
|Definition:||An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the WHRN gene on chromosome 9q32. https://www.ncbi.nlm.nih.gov/pubmed/12833159|
|Ontology:||Human Disease (DOID:0110490)|
|is a type of:||
OTHER autosomal recessive nonsyndromic deafness 31 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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