 Abnormalities, Multiple
"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.
No definition found.
| Descriptor ID |
D000015
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| MeSH Number(s) |
C16.131.077
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| Concept/Terms |
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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 |
|---|
| 1981 | 1 | 0 | 1 | | 1982 | 1 | 0 | 1 | | 1983 | 1 | 3 | 4 | | 1984 | 1 | 1 | 2 | | 1985 | 3 | 1 | 4 | | 1986 | 2 | 1 | 3 | | 1987 | 1 | 2 | 3 | | 1988 | 2 | 0 | 2 | | 1989 | 2 | 3 | 5 | | 1990 | 3 | 2 | 5 | | 1991 | 3 | 0 | 3 | | 1992 | 1 | 2 | 3 | | 1993 | 1 | 2 | 3 | | 1994 | 3 | 0 | 3 | | 1995 | 4 | 1 | 5 | | 1996 | 2 | 0 | 2 | | 1997 | 3 | 1 | 4 | | 1998 | 2 | 1 | 3 | | 1999 | 5 | 1 | 6 | | 2000 | 4 | 0 | 4 | | 2001 | 2 | 2 | 4 | | 2002 | 3 | 1 | 4 | | 2003 | 7 | 2 | 9 | | 2004 | 10 | 5 | 15 | | 2005 | 4 | 1 | 5 | | 2006 | 1 | 1 | 2 | | 2007 | 6 | 4 | 10 | | 2008 | 7 | 5 | 12 | | 2009 | 4 | 2 | 6 | | 2010 | 8 | 1 | 9 | | 2011 | 6 | 2 | 8 | | 2012 | 5 | 0 | 5 | | 2013 | 9 | 2 | 11 | | 2014 | 5 | 1 | 6 | | 2015 | 10 | 1 | 11 | | 2016 | 5 | 3 | 8 | | 2017 | 2 | 1 | 3 | | 2018 | 5 | 0 | 5 | | 2019 | 5 | 0 | 5 | | 2020 | 2 | 0 | 2 |
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Below are the most recent publications written about "Abnormalities, Multiple" by people in Profiles.
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Unlu G, Qi X, Gamazon ER, Melville DB, Patel N, Rushing AR, Hashem M, Al-Faifi A, Chen R, Li B, Cox NJ, Alkuraya FS, Knapik EW. Phenome-based approach identifies RIC1-linked Mendelian syndrome through zebrafish models, biobank associations and clinical studies. Nat Med. 2020 01; 26(1):98-109.
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Mak CCY, Doherty D, Lin AE, Vegas N, Cho MT, Viot G, Dimartino C, Weisfeld-Adams JD, Lessel D, Joss S, Li C, Gonzaga-Jauregui C, Zarate YA, Ehmke N, Horn D, Troyer C, Kant SG, Lee Y, Ishak GE, Leung G, Barone Pritchard A, Yang S, Bend EG, Filippini F, Roadhouse C, Lebrun N, Mehaffey MG, Martin PM, Apple B, Millan F, Puk O, Hoffer MJV, Henderson LB, McGowan R, Wentzensen IM, Pei S, Zahir FR, Yu M, Gibson WT, Seman A, Steeves M, Murrell JR, Luettgen S, Francisco E, Strom TM, Amlie-Wolf L, Kaindl AM, Wilson WG, Halbach S, Basel-Salmon L, Lev-El N, Denecke J, Vissers LELM, Radtke K, Chelly J, Zackai E, Friedman JM, Bamshad MJ, Nickerson DA. MN1 C-terminal truncation syndrome is a novel neurodevelopmental and craniofacial disorder with partial rhombencephalosynapsis. Brain. 2020 01 01; 143(1):55-68.
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Morris SA, Ghanayem NS. Patient With Poor Prognosis, Family Wishes to Pursue All Options, Care Team Cannot Reach Consensus. Ann Thorac Surg. 2019 11; 108(5):1284-1286.
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Amrom D, Poduri A, Goldman JS, Dan B, Deconinck N, Pichon B, Nadaf J, Andermann F, Andermann E, Walsh CA, Dobyns WB. Duplication 2p16 is associated with perisylvian polymicrogyria. Am J Med Genet A. 2019 12; 179(12):2343-2356.
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Elzein C, Abdulkarim M, Abbas U, Vricella L, Ilbawi M. Repair of Superior Sinus Venosus Atrial Septal Defect Using a Modified Two-Patch Technique. Ann Thorac Surg. 2020 02; 109(2):583-587.
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Kohli U. Isolated retroaortic innominate vein and right aortic arch: a case report and review of literature. Cardiol Young. 2019 Aug; 29(8):1091-1093.
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Gripp KW, Morse LA, Axelrad M, Chatfield KC, Chidekel A, Dobyns W, Doyle D, Kerr B, Lin AE, Schwartz DD, Sibbles BJ, Siegel D, Shankar SP, Stevenson DA, Thacker MM, Weaver KN, White SM, Rauen KA. Costello syndrome: Clinical phenotype, genotype, and management guidelines. Am J Med Genet A. 2019 09; 179(9):1725-1744.
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Moog U, Dobyns WB. An update on oculocerebrocutaneous (Delleman-Oorthuys) syndrome. Am J Med Genet C Semin Med Genet. 2018 12; 178(4):414-422.
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Piché J, Gosset N, Legault LM, Pacis A, Oneglia A, Caron M, Chetaille P, Barreiro L, Liu D, Qi X, Nattel S, Leclerc S, Breton-Larrivée M. Molecular Signature of CAID Syndrome: Noncanonical Roles of SGO1 in Regulation of TGF-ß Signaling and Epigenomics. Cell Mol Gastroenterol Hepatol. 2019; 7(2):411-431.
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Yap KL, Johnson AEK, Fischer D, Kandikatla P, Deml J, Nelakuditi V, Halbach S, Jeha GS, Burrage LC, Bodamer O, Benavides VC, Lewis AM, Ellard S, Shah P, Cody D, Diaz A, Devarajan A, Truong L, Greeley SAW, De Leó-Crutchlow DD, Edmondson AC, Das S, Thornton P, Waggoner D, Del Gaudio D. Congenital hyperinsulinism as the presenting feature of Kabuki syndrome: clinical and molecular characterization of 9 affected individuals. Genet Med. 2019 01; 21(1):233-242.
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