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Human Disease

autosomal dominant nonsyndromic deafness 56

Term ID
DOID:0110581
Synonyms
  • autosomal dominant deafness 56
  • DFNA56
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TNC gene on chromosome 9q33. https://www.ncbi.nlm.nih.gov/pubmed/23936043
References
Ontology
Human Disease   ( DOID:0110581 )
Relationships
is a type of
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Genes Involved
Zebrafish Models