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 20 ID (Ontology) DOID:0110550 (Human Disease)
Definition An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the ACTG1 gene on chromosome 17q25.
Also Known As "autosomal dominant deafness 20" ; "DFNA20" ; "DFNA26"
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 autosomal dominant nonsyndromic deafness 20       2
 for disease ribbon | autosomal dominant nonsyndromic deafness 20       2
 model of | autosomal dominant nonsyndromic deafness 20       2
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nonsyndromic deafness_______
autosomal dominant disease__|
                            autosomal dominant nonsyndromic deafness
                             |__autosomal dominant nonsyndromic deafness 20  2 rec.
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Is a autosomal dominant nonsyndromic deafness
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Synonyms
  • "autosomal dominant deafness 20" EXACT
    "DFNA20" EXACT OMO:0003012
    "DFNA26" EXACT OMO:0003012
Secondary IDs
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ICD10CM:H90.3
MIM:604717