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 28 ID (Ontology) DOID:0110557 (Human Disease)
Definition An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the GRHL2 gene on chromosome 8q22.
Also Known As "autosomal dominant deafness 28" ; "DFNA28"
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 autosomal dominant nonsyndromic deafness 28       1
 for disease ribbon | autosomal dominant nonsyndromic deafness 28       1
 model of | autosomal dominant nonsyndromic deafness 28       1
Spanning Tree (Parents/Children)
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nonsyndromic deafness_______
autosomal dominant disease__|
                            autosomal dominant nonsyndromic deafness
                             |__autosomal dominant nonsyndromic deafness 28  1 rec.
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Is a autosomal dominant nonsyndromic deafness
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Synonyms
  • "autosomal dominant deafness 28" EXACT
    "DFNA28" EXACT OMO:0003012
Secondary IDs
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ICD10CM:H90.3
MIM:608641