Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 68

Term ID
DOID:0110589
Synonyms
  • autosomal dominant deafness 68
  • DFNA68
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the HOMER2 gene on chromosome 15q25. https://www.ncbi.nlm.nih.gov/pubmed/25816005
References
Ontology
Human Disease   ( DOID:0110589 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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