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

• ICD10CM:H90.3
• OMIM:613916

Ontology

Human Disease   ( DOID:0110534 )