Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 11

Term ID
DOID:0110543
Synonyms
  • autosomal dominant deafness 11
  • DFNA11
Definition
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the MYO7A gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/9354784
References
Ontology
Human Disease   ( DOID:0110543 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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