OBO ID: DOID:0110559 |
Term Name: | autosomal dominant nonsyndromic deafness 2B | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0110559 ) |
OTHER autosomal dominant nonsyndromic deafness 2B PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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