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Nonsyndromic deafness

What is nonsyndromic deafness? A clear definition from the hearing section of our glossary, with 14 related terms, tools to try and further reading.

Definition of Nonsyndromic deafness

Nonsyndromic deafness is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Nonsyndromic deafness constitutes 75% of all hearing loss cases, and an estimated 100 genes are thought to be linked to this condition. About 80% are linked to autosomal recessive inheritance, 15% to autosomal dominant inheritance, 1-3% through the X chromosome, and 0.5-1% are associated with mitochondrial inheritance.

Genetic changes are related to the following types of nonsyndromic deafness:

DFNA: nonsyndromic deafness, autosomal dominant

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What is Nonsyndromic deafness?

Nonsyndromic deafness is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body.

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