OBO ID: DOID:0110481
Term Name: autosomal recessive nonsyndromic deafness 23 Search Ontology:
Synonyms:
  • autosomal recessive deafness 23
  • DFNB23
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the PCDH15 gene on chromosome 10q21. https://www.ncbi.nlm.nih.gov/pubmed/14570705
References:
Ontology: Human Disease   (DOID:0110481)
OTHER autosomal recessive nonsyndromic deafness 23 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
PCDH15 Deafness, autosomal recessive 23 609533
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None