Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 13

Term ID
DOID:0110468
Synonyms
  • autosomal recessive deafness 13
  • DFNB13
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 7q34-q36. https://www.ncbi.nlm.nih.gov/pubmed/9781028
References
Ontology
Human Disease   ( DOID:0110468 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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