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

Molecular Interaction Atlas (MIA)
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.