OBO ID: DOID:0110490
Term Name: autosomal recessive nonsyndromic deafness 31 Search Ontology:
Synonyms:
  • autosomal recessive deafness 31
  • DFNB31
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the WHRN gene on chromosome 9q32. https://www.ncbi.nlm.nih.gov/pubmed/12833159
References:
Ontology: Human Disease   (DOID:0110490)
OTHER autosomal recessive nonsyndromic deafness 31 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
WHRN Deafness, autosomal recessive 31 607084
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None