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ZIRC
OBO ID: DOID:0110497
Term Name: autosomal recessive nonsyndromic deafness 39 Search Ontology:
Synonyms:
  • autosomal recessive deafness 39
  • DFNB39
Definition: An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, downsloping hearing loss and has_material_basis_in mutation in the HGF gene on chromosome 7q21.https://www.ncbi.nlm.nih.gov/pubmed/19576567
References:
Ontology: Human Disease   (DOID:0110497)
OTHER autosomal recessive nonsyndromic deafness 39 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
HGF Deafness, autosomal recessive 39 608265
ZEBRAFISH MODELSNo data available
PHENOTYPE No data available

CITATIONS: None