Details of Disease

General Information of Disease (ID: DISW62TK)

• Disease Name: Autosomal recessive nonsyndromic hearing loss 37
• Synonyms: deafness, autosomal recessive 37; autosomal recessive nonsyndromic deafness type 37; deafness, autosomal recessive type 37; autosomal recessive deafness 37; autosomal recessive nonsyndromic deafness 37; autosomal recessive nonsyndromic deafness caused by mutation in MYO6; DFNB37; MYO6 autosomal recessive nonsyndromic deafness; autosomal recessive nonsyndromic hearing loss 37
• Definition: Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO6 gene.
• Disease Hierarchy:
  DIS8G9R9: Hearing loss, autosomal recessive
  DISW62TK: Autosomal recessive nonsyndromic hearing loss 37
• Disease Identifiers:
  MONDO ID: MONDO_0011912
  MESH ID: C564331
  UMLS CUI: C1843028
  OMIM ID: 607821
  MedGen ID: 375076

Molecular Interaction Atlas (MIA) of This Disease

This Disease Is Related to 1 DOT Molecule(s)

Gene Name	DOT ID	Evidence Level	Mode of Inheritance	REF
MYO6	OTJQYRC7	Strong	Autosomal recessive	[1]

References

• [1] Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing. Eur J Hum Genet. 2014 Jun;22(6):768-75. doi: 10.1038/ejhg.2013.232. Epub 2013 Oct 9.