Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 96

Term ID
DOID:0110538
Synonyms
  • autosomal recessive deafness 96
  • DFNB96
Definition
An autosomal recessive nonsyndromic deafness that has_material_basis_in variation in the chromosome region 1p36.31-p36.13. https://www.ncbi.nlm.nih.gov/pubmed/21937999
References
Ontology
Human Disease   ( DOID:0110538 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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