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Human Disease

autosomal recessive nonsyndromic deafness 33

Term ID
DOID:0110492
Synonyms
  • autosomal recessive deafness 33
  • DFNB33
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 10p11.23-q21.1. https://www.ncbi.nlm.nih.gov/pubmed/12080392
References
Ontology
Human Disease   ( DOID:0110492 )
Relationships
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Genes Involved
Zebrafish Models