Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 50

Term ID
DOID:0110576
Synonyms
  • autosomal dominant deafness 50
  • DFNA50
Definition
An autosomal dominant nonsyndromic deafness that is characterized postlingual onset in the second decade of life with flat progressive hearing loss and has_material_basis_in mutation in the MIRN96 gene on chromosome 7q32. https://www.ncbi.nlm.nih.gov/pubmed/19363479
References
Ontology
Human Disease   ( DOID:0110576 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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