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Human Disease

autosomal dominant nonsyndromic deafness 13

Term ID
DOID:0110545
Synonyms
  • autosomal dominant deafness 13
  • DFNA13
Definition
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has_material_basis_in mutation in the COL11A2 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/10581026
References
Ontology
Human Disease   ( DOID:0110545 )
Relationships
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Genes Involved
Zebrafish Models