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Human Disease

autosomal dominant nonsyndromic deafness 25

Term ID
DOID:0110555
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
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Genes Involved
Zebrafish Models