OBO ID: DOID:0110571
Term Name: autosomal dominant nonsyndromic deafness 48 Search Ontology:
Synonyms:
  • autosomal dominant deafness 48
  • DFNA48
Definition: An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with progressive hearing loss and has_material_basis_in variation in the chromosome region 12q13-q14. https://www.ncbi.nlm.nih.gov/pubmed/12736868
References:
Ontology: Human Disease   ( DOID:0110571 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 48 PAGES
GENES INVOLVED No data available
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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