FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autosomal dominant nonsyndromic deafness 86 ID (Ontology) DOID:0070610 (Human Disease)
Definition An autosomal dominant nonsyndromic deafness characterized by late-onset progressive hearing loss through p53-mediated hair cell apoptosis that has_material_basis_in heterozygous mutation in the THOC1 gene on chromosome 18p11.
Also Known As "autosomal dominant deafness 86" ; "DFNA86"
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 autosomal dominant nonsyndromic deafness 86       1
 for disease ribbon | autosomal dominant nonsyndromic deafness 86       1
 model of | autosomal dominant nonsyndromic deafness 86       1
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nonsyndromic deafness_______
autosomal dominant disease__|
                            autosomal dominant nonsyndromic deafness
                             |__autosomal dominant nonsyndromic deafness 86  1 rec.
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Is a autosomal dominant nonsyndromic deafness
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Synonyms
  • "autosomal dominant deafness 86" EXACT
    "DFNA86" EXACT OMO:0003012
Secondary IDs
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MIM:620280