Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 76

Term ID
DOID:0110524
Synonyms
  • autosomal recessive deafness 76
  • DFNB76
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with high frequency, progressive hearing loss and has_material_basis_in mutation in the SYNE4 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/23348741
References
Ontology
Human Disease   ( DOID:0110524 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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