OBO ID: DOID:0110559
Term Name: autosomal dominant nonsyndromic deafness 2B Search Ontology:
Synonyms:
  • autosomal dominant deafness 2B
  • DFNA2B
Definition: An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the fourth decade of life with by high frequency progressive hearing loss and has_material_basis_in mutation in the GJB3 gene on chromosome 1p34.3. https://www.ncbi.nlm.nih.gov/pubmed/9843210
References:
Ontology: Human Disease   ( DOID:0110559 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 2B PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
GJB3 Deafness, autosomal dominant 2B 612644
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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