OBO ID: DOID:0110576
Term Name: autosomal dominant nonsyndromic deafness 50 Search Ontology:
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 autosomal dominant nonsyndromic deafness 50 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MIR96