OBO ID: DOID:0110517
Term Name: autosomal recessive nonsyndromic deafness 66 Search Ontology:
Synonyms:
  • autosomal recessive deafness 66
  • DFNB66
Definition: An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the DCDC2 gene on chromosome 6p22. https://www.ncbi.nlm.nih.gov/pubmed/25601850
References:
Ontology: Human Disease   ( DOID:0110517 )
OTHER autosomal recessive nonsyndromic deafness 66 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
DCDC2 ?Deafness, autosomal recessive 66
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None