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Human Disease

autosomal dominant nonsyndromic deafness 15

Term ID
DOID:0110546
Synonyms
  • autosomal dominant deafness 15
  • DFNA15
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 POU4F3 gene on chromosome 5q32. https://www.ncbi.nlm.nih.gov/pubmed/9506947
References
Ontology
Human Disease   ( DOID:0110546 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations