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Human Disease

autosomal recessive nonsyndromic deafness 39

Term ID
DOID:0110497
Synonyms
  • autosomal recessive deafness 39
  • DFNB39
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21. https://www.ncbi.nlm.nih.gov/pubmed/19576567
References
Ontology
Human Disease   ( DOID:0110497 )
Relationships
is a type of
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Genes Involved
Zebrafish Models