"Hearing Loss" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A general term for the complete or partial loss of the ability to hear from one or both ears.
Descriptor ID |
D034381
|
MeSH Number(s) |
C09.218.458.341 C10.597.751.418.341 C23.888.592.763.393.341
|
Concept/Terms |
Hearing Loss- Hearing Loss
- Loss, Hearing
- Hypoacusis
- Hypoacuses
- Hearing Impairment
|
Below are MeSH descriptors whose meaning is more general than "Hearing Loss".
Below are MeSH descriptors whose meaning is more specific than "Hearing Loss".
This graph shows the total number of publications written about "Hearing Loss" by people in this website by year, and whether "Hearing Loss" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
---|
2002 | 1 | 0 | 1 |
2006 | 0 | 1 | 1 |
2011 | 1 | 0 | 1 |
2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hearing Loss" by people in Profiles.
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Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran. Clin Genet. 2021 07; 100(1):59-78.
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Nonsense mutations in SMPX, encoding a protein responsive to physical force, result in X-chromosomal hearing loss. Am J Hum Genet. 2011 May 13; 88(5):621-7.
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Oculo-oto-facial dysplasia (OOFD) versus Burn-McKeown syndrome. Am J Med Genet A. 2006 Nov 01; 140(21):2381-2; author reply 2383-4.
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A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10. Mol Med. 2002 Oct; 8(10):607-11.