OBO ID: DOID:0110555
Term Name: autosomal dominant nonsyndromic deafness 25 Search Ontology:
Synonyms:
  • autosomal dominant deafness 25
  • DFNA25
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second-sixth decade of life with high frequency progressive hearing loss and has_material_basis_in mutation in the SLC17A8 gene on chromosome 12q23. https://www.ncbi.nlm.nih.gov/pubmed/18674745
References:
Ontology: Human Disease   ( DOID:0110555 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 25 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC17A8 Deafness, autosomal dominant 25 605583
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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