Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 66

Term ID
DOID:0110587
Synonyms
  • autosomal dominant deafness 66
  • DFNA66
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CD164 gene on chromosome 6q21. https://www.ncbi.nlm.nih.gov/pubmed/26197441
References
Ontology
Human Disease   ( DOID:0110587 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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