Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 1B

Term ID
DOID:0110476
Synonyms
  • autosomal recessive deafness 1B
  • DFNB1B
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually stable hearing loss and has_material_basis_in mutation in the GJB6 gene on chromosome 13q12. https://www.ncbi.nlm.nih.gov/pubmed/11807148
References
Ontology
Human Disease   ( DOID:0110476 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models