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Human Disease

autosomal dominant nonsyndromic deafness 10

Term ID
DOID:0110542
Synonyms
  • autosomal dominant deafness 10
  • DFNA10
Definition
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the third or forth decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the EYA4 gene on chromosome 6q23. https://www.ncbi.nlm.nih.gov/pubmed/11159937
References
Ontology
Human Disease   ( DOID:0110542 )
Relationships
is a type of
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Genes Involved
Zebrafish Models
Citations