OBO ID: DOID:0110527
Term Name: autosomal recessive nonsyndromic deafness 8 Search Ontology:
Synonyms:
  • autosomal recessive deafness 10
  • autosomal recessive deafness 8
  • childhood-onset neurosensory autosomal recessive deafness 8
  • DFNB10
  • DFNB8
  • neurosensory nonsyndromic recessive deafness 8
  • NRSD8
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the TMPRSS3 gene on chromosome 21q22. https://www.ncbi.nlm.nih.gov/pubmed/11137999
References:
Ontology: Human Disease   ( DOID:0110527 )
OTHER autosomal recessive nonsyndromic deafness 8 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
TMPRSS3 Deafness, autosomal recessive 8/10 601072
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None