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Human Disease

autosomal dominant nonsyndromic deafness 23

Term ID
DOID:0110553
Synonyms
  • autosomal dominant deafness 23
  • DFNA23
Definition
An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the SIX1 gene on chromosome 14q23. https://www.ncbi.nlm.nih.gov/pubmed/15141091
References
Ontology
Human Disease   ( DOID:0110553 )
Relationships
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Genes Involved
Zebrafish Models