Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 91

Term ID
DOID:0110536
Synonyms
  • autosomal recessive deafness 91
  • DFNB91
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the SERPINB6 gene on chromosome 6p25. https://www.ncbi.nlm.nih.gov/pubmed/20451170
References
Ontology
Human Disease   ( DOID:0110536 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models