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 89 ID (Ontology) DOID:0070612 (Human Disease)
Definition An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ATOH1 gene on chromosome 4q22.
Also Known As "autosomal dominant deafness 89" ; "DFNA89"
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 Genes
 autosomal dominant nonsyndromic deafness 89       3
 for disease ribbon | autosomal dominant nonsyndromic deafness 89       3
 model of | autosomal dominant nonsyndromic deafness 89       3
Spanning Tree (Parents/Children)
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nonsyndromic deafness_______
autosomal dominant disease__|
                            autosomal dominant nonsyndromic deafness
                             |__autosomal dominant nonsyndromic deafness 89  3 rec.
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Is a autosomal dominant nonsyndromic deafness
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Synonyms
  • "autosomal dominant deafness 89" EXACT
    "DFNA89" EXACT OMO:0003012
Secondary IDs
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MIM:620284