OBO ID: DOID:0111735 |
Term Name: | X-linked deafness 4 | Search Ontology: | |
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Definition: | An X-linked nonsyndromic deafness characterized by progressive hearing loss with postlingual onset and earlier onset in males compared to females that has_material_basis_in mutation in the SMPX gene on chromosome Xp22.12. https://www.ncbi.nlm.nih.gov/pubmed/8872482 | ||
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Ontology: | Human Disease ( DOID:0111735 ) |
OTHER X-linked deafness 4 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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