OBO ID: DOID:0110515
Term Name: autosomal recessive nonsyndromic deafness 63 Search Ontology:
Synonyms:
  • autosomal recessive deafness 63
  • DFNB63
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 LRTOMT gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/18953341
References:
Ontology: Human Disease   ( DOID:0110515 )
Relationships
is a type of:
OTHER autosomal recessive nonsyndromic deafness 63 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
LRTOMT Deafness, autosomal recessive 63
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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