Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 9

Term ID
DOID:0110535
Synonyms
  • autosomal recessive deafness 9
  • DFNB9
  • neurosensory nonsyndromic recessive deafness 9
  • NRSD9
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOF gene on chromosome 2p23. https://www.ncbi.nlm.nih.gov/pubmed/10192385
References
Ontology
Human Disease   ( DOID:0110535 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models