OBO ID: DOID:0110574 |
Term Name: | autosomal dominant nonsyndromic deafness 4B | Search Ontology: | |
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Synonyms: |
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Definition: | An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CEACAM16 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/21368133 | ||
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Ontology: | Human Disease ( DOID:0110574 ) |
OTHER autosomal dominant nonsyndromic deafness 4B PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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CEACAM16 | Deafness, autosomal dominant 4B |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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