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Human Disease
autosomal recessive nonsyndromic deafness 89
- Term ID
- DOID:0110534
- Synonyms
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- 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
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- ICD10CM:H90.3
- MIM:613916
- Ontology
- Human Disease ( DOID:0110534 )
- is a type of
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