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 125 ID (Ontology) DOID:0061124 (Human Disease)
Definition An autosomal recessive nonsyndromic deafness characterized by congenital nonsyndromic sensorineural hearing loss hat has_material_basis_in homozygous mutation in the GAS2 gene on chromosome 11p14." [url:https\://pubmed.ncbi.nlm.nih.gov/33964205/] {comment="Only 1 family has been reported as of 4/17/2025"}
Also Known As "autosomal recessive deafness 125" ; "DFNB125"
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 Genes
 autosomal recessive nonsyndromic deafness 125       1
 for disease ribbon | autosomal recessive nonsyndromic deafness 125       1
 model of | autosomal recessive nonsyndromic deafness 125       1
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nonsyndromic deafness________
autosomal recessive disease__|
                             autosomal recessive nonsyndromic deafness
                              |__autosomal recessive nonsyndromic deafness 125  1 rec.
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Is a autosomal recessive nonsyndromic deafness
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Synonyms
  • "autosomal recessive deafness 125" EXACT
    "DFNB125" EXACT OMO:0003012
Secondary IDs
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MIM:620877