OBO ID: DOID:0110543
Term Name: autosomal dominant nonsyndromic deafness 11 Search Ontology:
Synonyms:
  • autosomal dominant deafness 11
  • DFNA11
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the first decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the MYO7A gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/9354784
References:
Ontology: Human Disease   ( DOID:0110543 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 11 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MYO7A Deafness, autosomal dominant 11 601317
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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