|OBO ID: DOID:0110512|
|Term Name:||autosomal recessive nonsyndromic deafness 6||Search Ontology:|
|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|
|Ontology:||Human Disease (DOID:0110512)|
|is a type of:||
OTHER autosomal recessive nonsyndromic deafness 6 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
Your Input Welcome
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.