Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 3B

Term ID
DOID:0110565
Synonyms
  • autosomal dominant deafness 3B
  • DFNA3B
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the GJB6 gene on chromosome 13q12. https://www.ncbi.nlm.nih.gov/pubmed/10471490
References
Ontology
Human Disease   ( DOID:0110565 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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