OBO ID: DOID:0110487
Term Name: autosomal recessive nonsyndromic deafness 29 Search Ontology:
Synonyms:
  • autosomal recessive deafness 29
  • DFNB29
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 CLDN14 gene on chromosome 21q22. https://www.ncbi.nlm.nih.gov/pubmed/11163249
References:
Ontology: Human Disease   ( DOID:0110487 )
Relationships
is a type of:
OTHER autosomal recessive nonsyndromic deafness 29 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
CLDN14 Deafness, autosomal recessive 29
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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