OBO ID: DOID:0110512
Term Name: autosomal recessive nonsyndromic deafness 6 Search Ontology:
Synonyms:
  • autosomal recessive deafness 6
  • DFNB6
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the TMIE gene on chromosome 3p21. https://www.ncbi.nlm.nih.gov/pubmed/12145746
References:
Ontology: Human Disease   (DOID:0110512)
OTHER autosomal recessive nonsyndromic deafness 6 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TMIE Deafness, autosomal recessive 6 600971
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None