|OBO ID: DOID:0110481|
|Term Name:||autosomal recessive nonsyndromic deafness 23||Search Ontology:|
|Definition:||An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the PCDH15 gene on chromosome 10q21. https://www.ncbi.nlm.nih.gov/pubmed/14570705|
|Ontology:||Human Disease (DOID:0110481)|
|is a type of:||
OTHER autosomal recessive nonsyndromic deafness 23 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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