OBO ID: DOID:0110513
Term Name: autosomal recessive nonsyndromic deafness 61 Search Ontology:
Synonyms:
  • autosomal recessive deafness 61
  • DFNB61
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 SLC26A5 gene on chromosome 7q22. https://www.ncbi.nlm.nih.gov/pubmed/12719379
References:
Ontology: Human Disease   ( DOID:0110513 )
OTHER autosomal recessive nonsyndromic deafness 61 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC26A5 ?Deafness, autosomal recessive 61 613865
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None