OBO ID: DOID:0110563
Term Name: autosomal dominant nonsyndromic deafness 36 Search Ontology:
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 autosomal dominant nonsyndromic deafness 36 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TMC1 Deafness, autosomal dominant 36 606705
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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