OBO ID: DOID:0110471
Term Name: autosomal recessive nonsyndromic deafness 16 Search Ontology:
Synonyms:
  • autosomal recessive deafness 16
  • DFNB16
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 STRC gene on chromosome 15q15. https://www.ncbi.nlm.nih.gov/pubmed/11687802
References:
Ontology: Human Disease   (DOID:0110471)
Relationships
is a type of:
OTHER autosomal recessive nonsyndromic deafness 16 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
STRC Deafness, autosomal recessive 16
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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