OBO ID: DOID:0111636 |
Term Name: | autosomal recessive nonsyndromic deafness 113 | Search Ontology: | |
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Definition: | An autosomal recessive nonsyndromic deafness characterized by postlingual progressive hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in the CEACAM16 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/29703829 | ||
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Ontology: | Human Disease ( DOID:0111636 ) |
OTHER autosomal recessive nonsyndromic deafness 113 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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CEACAM16 | Deafness, autosomal recessive 113 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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