OBO ID: DOID:0110494
Term Name: autosomal recessive nonsyndromic deafness 36 Search Ontology:
Synonyms:
  • autosomal recessive deafness 36
  • DFNB36
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the ESPN gene on chromosome 1p36. https://www.ncbi.nlm.nih.gov/pubmed/15286153
References:
Ontology: Human Disease   ( DOID:0110494 )
OTHER autosomal recessive nonsyndromic deafness 36 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ESPN Deafness, neurosensory, without vestibular involvement, autosomal dominant 609006
Deafness, autosomal recessive 36 609006
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None