OBO ID: DOID:0110550
Term Name: autosomal dominant nonsyndromic deafness 20 Search Ontology:
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
is a type of:
OTHER autosomal dominant nonsyndromic deafness 20 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ACTG1 Deafness, autosomal dominant 20/26
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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