FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autosomal recessive nonsyndromic deafness 61 ID (Ontology) DOID:0110513 (Human Disease)
Definition An autosomal recessive nonsyndromic deafness that is characterized by early childhood-onset moderate to severe sensorineural hearing loss and has_material_basis_in mutation in the SLC26A5 gene on chromosome 7q22.
Also Known As "autosomal recessive deafness 61" ; "DFNB61"
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 Genes
 autosomal recessive nonsyndromic deafness 61       1
 for disease ribbon | autosomal recessive nonsyndromic deafness 61       1
 model of | autosomal recessive nonsyndromic deafness 61       1
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nonsyndromic deafness________
autosomal recessive disease__|
                             autosomal recessive nonsyndromic deafness
                              |__autosomal recessive nonsyndromic deafness 61  1 rec.
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Is a autosomal recessive nonsyndromic deafness
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Synonyms
  • "autosomal recessive deafness 61" EXACT
    "DFNB61" EXACT OMO:0003012
Secondary IDs
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ICD10CM:H90.3
MIM:613865