"Abnormalities, Multiple" 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 abnormalities that affect more than one organ or body structure.
Descriptor ID |
D000015
|
MeSH Number(s) |
C16.131.077
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Abnormalities, Multiple".
Below are MeSH descriptors whose meaning is more specific than "Abnormalities, Multiple".
This graph shows the total number of publications written about "Abnormalities, Multiple" by people in this website by year, and whether "Abnormalities, Multiple" 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 |
---|
1994 | 4 | 0 | 4 |
1995 | 6 | 0 | 6 |
1996 | 7 | 1 | 8 |
1997 | 8 | 2 | 10 |
1998 | 8 | 6 | 14 |
1999 | 6 | 0 | 6 |
2000 | 8 | 5 | 13 |
2001 | 4 | 1 | 5 |
2002 | 6 | 2 | 8 |
2003 | 10 | 3 | 13 |
2004 | 8 | 3 | 11 |
2005 | 26 | 3 | 29 |
2006 | 14 | 5 | 19 |
2007 | 28 | 6 | 34 |
2008 | 18 | 8 | 26 |
2009 | 17 | 13 | 30 |
2010 | 21 | 11 | 32 |
2011 | 11 | 10 | 21 |
2012 | 13 | 11 | 24 |
2013 | 12 | 10 | 22 |
2014 | 20 | 3 | 23 |
2015 | 13 | 7 | 20 |
2016 | 13 | 6 | 19 |
2017 | 11 | 1 | 12 |
2018 | 11 | 3 | 14 |
2019 | 12 | 12 | 24 |
2020 | 15 | 2 | 17 |
2021 | 15 | 3 | 18 |
2022 | 8 | 2 | 10 |
2023 | 4 | 0 | 4 |
To return to the timeline,
click here.
Below are the most recent publications written about "Abnormalities, Multiple" by people in Profiles.
-
Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return. Eur J Hum Genet. 2023 12; 31(12):1430-1439.
-
A non-coding insertional mutation of Grhl2 causes gene over-expression and multiple structural anomalies including cleft palate, spina bifida and encephalocele. Hum Mol Genet. 2023 08 26; 32(17):2681-2692.
-
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays. Eur J Hum Genet. 2023 10; 31(10):1117-1124.
-
Facial analytics based on a coordinate extrapolation system (zFACE) for morphometric phenotyping of developing zebrafish. Dis Model Mech. 2023 06 01; 16(6).
-
Patterns of co-occurring birth defects in children with anotia and microtia. Am J Med Genet A. 2023 03; 191(3):805-812.
-
Koolen-de Vries syndrome associated with continuous spike-wave in sleep Epileptic Disord. 2022 10 01; 24(5):928-933.
-
Long read sequencing and expression studies of AHDC1 deletions in Xia-Gibbs syndrome reveal a novel genetic regulatory mechanism. Hum Mutat. 2022 12; 43(12):2033-2053.
-
Reply to "Comment: Another Piece of the Puzzle of Anomalous Connectivity in Joubert's Syndrome". Neuropediatrics. 2022 08; 53(4):306-307.
-
Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic hernia. Am J Med Genet A. 2022 09; 188(9):2718-2723.
-
Clinical features and orbital anomalies in Fraser syndrome and a review of management options. Indian J Ophthalmol. 2022 07; 70(7):2559-2563.