OBO ID: DOID:0111641 |
Term Name: | autosomal recessive nonsyndromic deafness 94 | Search Ontology: | |
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Definition: | An autosomal recessive nonsyndromic deafness characterized by prelingual profound sensorineural hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the NARS2 gene on chromosome 11q14.1. https://www.ncbi.nlm.nih.gov/pubmed/25807530 | ||
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Ontology: | Human Disease ( DOID:0111641 ) |
OTHER autosomal recessive nonsyndromic deafness 94 PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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