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Human Disease

autosomal recessive nonsyndromic deafness 3

Term ID
DOID:0110488
Synonyms
  • autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3
  • DFNB3
  • NRSD3
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 MYO15A gene on chromosome 17p11. https://www.ncbi.nlm.nih.gov/pubmed/17851452
References
Ontology
Human Disease   ( DOID:0110488 )
Relationships
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Genes Involved
Zebrafish Models