OBO ID: DOID:0110552
Term Name: autosomal dominant nonsyndromic deafness 22 Search Ontology:
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
is a type of:
OTHER autosomal dominant nonsyndromic deafness 22 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MYO6 Deafness, autosomal dominant 22, with hypertrophic cardiomyopathy 606346
Deafness, autosomal dominant 22 606346
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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