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Human Disease

autosomal dominant nonsyndromic deafness 20

Term ID
DOID:0110550
Synonyms
  • autosomal dominant deafness 20
  • DFNA20
  • DFNA26
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. https://www.ncbi.nlm.nih.gov/pubmed/13680526
References
Ontology
Human Disease   ( DOID:0110550 )
Relationships
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Genes Involved
Zebrafish Models