OBO ID: DOID:0111636
Term Name: autosomal recessive nonsyndromic deafness 113 Search Ontology:
Synonyms:
  • autosomal recessive deafness 113
  • DFNB113
Definition: An autosomal recessive nonsyndromic deafness characterized by postlingual progressive hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in the CEACAM16 gene on chromosome 19q13. https://www.ncbi.nlm.nih.gov/pubmed/29703829
References:
Ontology: Human Disease   ( DOID:0111636 )
OTHER autosomal recessive nonsyndromic deafness 113 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CEACAM16 Deafness, autosomal recessive 113
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None