OBO ID: DOID:0080267 |
Term Name: | autosomal dominant nonsyndromic deafness 71 | Search Ontology: | |
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Definition: | An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the DMXL2 gene on chromosome 15q21. https://pubmed.ncbi.nlm.nih.gov/27657680/ | ||
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Ontology: | Human Disease ( DOID:0080267 ) |
OTHER autosomal dominant nonsyndromic deafness 71 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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