Search Ontology:
Human Disease

autosomal recessive nonsyndromic deafness 110

Term ID
DOID:0111644
Synonyms
  • autosomal recessive deafness 110
  • DFNB110
Definition
An autosomal recessive nonsyndromic deafness characterized by prelingual, bilateral hearing loss that has_material_basis_in homozygous or compound heterozygous mutation in the COCH gene on chromosome 14q12. https://www.ncbi.nlm.nih.gov/pubmed/29449721
References
Ontology
Human Disease   ( DOID:0111644 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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