Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 22

Term ID
DOID:0110552
Synonyms
  • autosomal dominant deafness 22
  • DFNA22
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 MYO6 gene on chromosome 6q14. https://www.ncbi.nlm.nih.gov/pubmed/11468689
References
Ontology
Human Disease   ( DOID:0110552 )
Relationships
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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