Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 9

Term ID
DOID:0110593
Synonyms
  • autosomal dominant deafness 9
  • DFNA9
Definition
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has_material_basis_in mutation in the COCH gene on chromosome 14q12. https://www.ncbi.nlm.nih.gov/pubmed/9806553
References
Ontology
Human Disease   ( DOID:0110593 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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