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Human Disease

autosomal recessive nonsyndromic deafness 18B

Term ID
DOID:0110474
Synonyms
  • autosomal recessive deafness 18B
  • DFNB18B
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the OTOG gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/23122587
References
Ontology
Human Disease   ( DOID:0110474 )
Relationships
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Genes Involved
Zebrafish Models