Search Ontology:
Human Disease

autosomal dominant nonsyndromic deafness 21

Term ID
DOID:0110551
Synonyms
  • autosomal dominant deafness 21
  • DFNA21
Definition
An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 6p24.1-p22.3. https://www.ncbi.nlm.nih.gov/pubmed/10764236
References
Ontology
Human Disease   ( DOID:0110551 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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