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Human Disease

autosomal recessive nonsyndromic deafness 89

Term ID
DOID:0110534
Synonyms
  • autosomal recessive deafness 89
  • DFNB89
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the KARS gene on chromosome 16q23. https://www.ncbi.nlm.nih.gov/pubmed/23768514
References
Ontology
Human Disease   ( DOID:0110534 )
Relationships
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Genes Involved
Zebrafish Models