OBO ID: DOID:0110572
Term Name: autosomal dominant nonsyndromic deafness 49 Search Ontology:
Synonyms:
  • autosomal dominant deafness 49
  • DFNA49
Definition: An autosomal dominant nonsyndromic deafness that is characterized by moderate loss for low and mid frequencies and mild loss for high frequencies and has_material_basis_in variation in the chromosome region 1q21-q23. https://www.ncbi.nlm.nih.gov/pubmed/14627674
References:
Ontology: Human Disease   ( DOID:0110572 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 49 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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