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Human Disease

autosomal recessive nonsyndromic deafness 8

Term ID
DOID:0110527
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 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models