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Human Disease

autosomal dominant nonsyndromic deafness 4B

Term ID
DOID:0110574
Synonyms
  • autosomal dominant deafness 4B
  • DFNA4B
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CEACAM16 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/21368133
References
Ontology
Human Disease   ( DOID:0110574 )
Relationships
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Genes Involved
Zebrafish Models