Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 48

Term ID
DOID:0110571
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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