OBO ID: DOID:0111740 |
Term Name: | X-linked deafness 6 | Search Ontology: | |
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Definition: | An X-linked nonsyndromic deafness characterized by severe bilateral sensorineural hearing loss with cochlear malformation in males and mild to moderate hearing loss in females with later onset that has_material_basis_in mutation in the COL4A6 gene on chromosome Xq22.3. https://www.ncbi.nlm.nih.gov/pubmed/23714752 | ||
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Ontology: | Human Disease ( DOID:0111740 ) |
OTHER X-linked deafness 6 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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