"Deafness" 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 loss of the ability to hear from both ears.
Descriptor ID |
D003638
|
MeSH Number(s) |
C09.218.458.341.186 C10.597.751.418.341.186 C23.888.592.763.393.341.186
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Deafness".
Below are MeSH descriptors whose meaning is more specific than "Deafness".
This graph shows the total number of publications written about "Deafness" by people in this website by year, and whether "Deafness" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
2005 | 1 | 1 | 2 |
2014 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2020 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Deafness" by people in Profiles.
-
Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss. Clin Genet. 2020 07; 98(1):32-42.
-
Identification of causative variants in TXNL4A in Burn-McKeown syndrome and isolated choanal atresia. Eur J Hum Genet. 2017 10; 25(10):1126-1133.
-
OSBPL2 encodes a protein of inner and outer hair cell stereocilia and is mutated in autosomal dominant hearing loss (DFNA67). Orphanet J Rare Dis. 2015 Feb 10; 10:15.
-
Compound heterozygosity of low-frequency promoter deletions and rare loss-of-function mutations in TXNL4A causes Burn-McKeown syndrome. Am J Hum Genet. 2014 Dec 04; 95(6):698-707.
-
Keratitis-ichthyosis-deafness syndrome in association with follicular occlusion triad. Eur J Dermatol. 2005 Sep-Oct; 15(5):347-52.
-
KID Syndrome: report of a Scandinavian patient with connexin-26 gene mutation. Acta Derm Venereol. 2005; 85(2):152-5.