"Cleft Lip" 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.
Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region.
| Descriptor ID |
D002971
|
| MeSH Number(s) |
C07.465.409.225 C07.465.525.164 C07.650.525.164 C16.131.850.525.164
|
| Concept/Terms |
Cleft Lip- Cleft Lip
- Cleft Lips
- Lip, Cleft
- Lips, Cleft
- Harelip
- Harelips
|
Below are MeSH descriptors whose meaning is more general than "Cleft Lip".
Below are MeSH descriptors whose meaning is more specific than "Cleft Lip".
This graph shows the total number of publications written about "Cleft Lip" by people in this website by year, and whether "Cleft Lip" 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 |
|---|
| 1995 | 1 | 0 | 1 |
| 2009 | 6 | 0 | 6 |
| 2010 | 4 | 0 | 4 |
| 2011 | 3 | 1 | 4 |
| 2012 | 7 | 0 | 7 |
| 2013 | 4 | 1 | 5 |
| 2014 | 5 | 0 | 5 |
| 2015 | 5 | 0 | 5 |
| 2016 | 4 | 1 | 5 |
| 2017 | 6 | 0 | 6 |
| 2018 | 5 | 0 | 5 |
| 2019 | 4 | 1 | 5 |
| 2020 | 2 | 1 | 3 |
| 2021 | 4 | 0 | 4 |
| 2022 | 3 | 0 | 3 |
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Below are the most recent publications written about "Cleft Lip" by people in Profiles.
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Identification of de novo variants in nonsyndromic cleft lip with/without cleft palate patients with low polygenic risk scores. Mol Genet Genomic Med. 2023 03; 11(3):e2109.
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Prioritization of non-coding elements involved in non-syndromic cleft lip with/without cleft palate through genome-wide analysis of de novo mutations. HGG Adv. 2023 01 12; 4(1):100166.
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Allele-specific transcription factor binding in a cellular model of orofacial clefting. Sci Rep. 2022 02 02; 12(1):1807.
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TP63-related disorders: two case reports and a brief review of the literature. Dermatol Online J. 2021 Nov 15; 27(11).
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Familial cleft tongue caused by a unique translation initiation codon variant in TP63. Eur J Hum Genet. 2022 02; 30(2):211-218.
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MiRNA-149 as a Candidate for Facial Clefting and Neural Crest Cell Migration. J Dent Res. 2022 03; 101(3):323-330.
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Extending the allelic spectrum at noncoding risk loci of orofacial clefting. Hum Mutat. 2021 08; 42(8):1066-1078.
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Cleft lip/palate and educational attainment: cause, consequence or correlation? A Mendelian randomization study. Int J Epidemiol. 2020 08 01; 49(4):1282-1293.
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Evaluating shared genetic influences on nonsyndromic cleft lip/palate and oropharyngeal neoplasms. Genet Epidemiol. 2020 11; 44(8):924-933.
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Msx1 deficiency interacts with hypoxia and induces a morphogenetic regulation during mouse lip development. Development. 2020 06 24; 147(21).
MeSH information
