OBO ID: DOID:0110462 |
Term Name: | autosomal recessive nonsyndromic deafness 101 | Search Ontology: | |
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Synonyms: |
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Definition: | An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GRXCR2 gene on chromosome 5q32. https://www.ncbi.nlm.nih.gov/pubmed/24619944 | ||
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Ontology: | Human Disease ( DOID:0110462 ) |
OTHER autosomal recessive nonsyndromic deafness 101 PAGES
GENES INVOLVED
Human Gene | Zebrafish Ortholog | OMIM Term | OMIM Phenotype ID |
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GRXCR2 | ?Deafness, autosomal recessive 101 |
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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