Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 36

Term ID
DOID:0110563
Synonyms
  • autosomal dominant deafness 36
  • DFNA36
Definition
An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently downsloping audioprofiles and has_material_basis_in mutation in the TMC1 gene on chromosome 9q21. https://www.ncbi.nlm.nih.gov/pubmed/11850618
References
Ontology
Human Disease   ( DOID:0110563 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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