Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 67

Term ID
DOID:0110588
Synonyms
  • autosomal dominant deafness 67
  • DFNA67
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the OSBPL2 gene on chromosome 20q13. https://www.ncbi.nlm.nih.gov/pubmed/25077649
References
Ontology
Human Disease   ( DOID:0110588 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models