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Human Disease

autosomal recessive nonsyndromic deafness 37

Term ID
DOID:0110495
Synonyms
  • autosomal recessive deafness 37
  • DFNB37
Definition
An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14. https://www.ncbi.nlm.nih.gov/pubmed/12687499
References
Ontology
Human Disease   ( DOID:0110495 )
Relationships
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Genes Involved
Zebrafish Models