Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 35

Term ID
DOID:0110493
Synonyms
  • autosomal recessive deafness 35
  • DFNB35
Definition
An autosomal recessive nonsyndromic deafness that is characterized severe to profound hearing loss and has_material_basis_in mutation in the ESRRB gene on chromosome 14q24. https://www.ncbi.nlm.nih.gov/pubmed/18179891
References
Ontology
Human Disease   ( DOID:0110493 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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