Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 31

Term ID
DOID:0110561
Synonyms
  • autosomal dominant deafness 31
  • DFNA31
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 6p21.3. https://www.ncbi.nlm.nih.gov/pubmed/11559344
References
Ontology
Human Disease   ( DOID:0110561 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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