Details of Disease
General Information of Disease (ID: DISW62TK)
Disease Name | Autosomal recessive nonsyndromic hearing loss 37 | |||||
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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
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Definition | Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the MYO6 gene. | |||||
Disease Hierarchy | ||||||
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Molecular Interaction Atlas (MIA) of This Disease
Molecular Interaction Atlas (MIA) | |||||||||||||||||||||||||
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This Disease Is Related to 1 DOT Molecule(s)
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