|OBO ID: DOID:0110497|
|Term Name:||autosomal recessive nonsyndromic deafness 39||Search Ontology:|
|Definition:||An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21. https://www.ncbi.nlm.nih.gov/pubmed/19576567|
|Ontology:||Human Disease (DOID:0110497)|
|is a type of:||
OTHER autosomal recessive nonsyndromic deafness 39 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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