Chromosome Deletion

"Chromosome Deletion" 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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

Actual loss of portion of a chromosome.

Descriptor ID	D002872
MeSH Number(s)	C23.550.210.050.500.500 G05.365.590.029.530.175 G05.365.590.175.050.500.500 G05.365.590.762.180 G05.558.800.180 G05.700.131.500.500
Concept/Terms	Chromosome Deletion Chromosome Deletion Deletion, Chromosome Deletions, Chromosome Partial Monosomy Partial Monosomy Monosomies, Partial Partial Monosomies Monosomy, Partial

Below are MeSH descriptors whose meaning is more general than "Chromosome Deletion".

Diseases [C]
Pathological Conditions, Signs and Symptoms [C23]
Pathologic Processes [C23.550]
Chromosome Aberrations [C23.550.210]
Aneuploidy [C23.550.210.050]
Monosomy [C23.550.210.050.500]
Chromosome Deletion [C23.550.210.050.500.500]
Biological Sciences [G]
Genetic Phenomena [G05]
Genetic Variation [G05.365]
Mutation [G05.365.590]
Allelic Imbalance [G05.365.590.029]
Loss of Heterozygosity [G05.365.590.029.530]
Chromosome Deletion [G05.365.590.029.530.175]
Chromosome Aberrations [G05.365.590.175]
Aneuploidy [G05.365.590.175.050]
Monosomy [G05.365.590.175.050.500]
Chromosome Deletion [G05.365.590.175.050.500.500]
Sequence Deletion [G05.365.590.762]
Chromosome Deletion [G05.365.590.762.180]
Mutagenesis [G05.558]
Sequence Deletion [G05.558.800]
Chromosome Deletion [G05.558.800.180]
Ploidies [G05.700]
Aneuploidy [G05.700.131]
Monosomy [G05.700.131.500]
Chromosome Deletion [G05.700.131.500.500]

Below are MeSH descriptors whose meaning is related to "Chromosome Deletion".

Below are MeSH descriptors whose meaning is more specific than "Chromosome Deletion".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Chromosome Deletion" by people in this website by year, and whether "Chromosome Deletion" was a major or minor topic of these publications.

Bar chart showing 44 publications over 23 distinct years, with a maximum of 4 publications in 2009

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
1998	1	2	3
1999	1	0	1
2002	1	0	1
2003	3	0	3
2004	2	0	2
2005	2	1	3
2006	2	1	3
2007	1	1	2
2008	2	0	2
2009	4	0	4
2011	1	2	3
2012	0	1	1
2013	0	1	1
2014	1	0	1
2016	1	1	2
2017	0	2	2
2018	0	1	1
2019	0	1	1
2020	0	2	2
2021	0	1	1
2022	0	2	2
2023	0	2	2
2024	0	1	1

Below are the most recent publications written about "Chromosome Deletion" by people in Profiles.

Frusone V, Maurer K, Emanuel BS, McDonald-McGinn D, Sullivan KE. Inflammatory Proteomic Analysis of 22q11.2 Deletion Syndrome. J Clin Immunol. 2024 Mar 15; 44(3):82.

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Bhattarai D, McGinn DE, Crowley TB, Giunta V, Gaiser K, Zackai EH, Emanuel BS, Heimall J, Jyonouchi S, Lee J, Sun D, McDonald-McGinn DM, Sullivan KE. Immunologic, Molecular, and Clinical Profile of Patients with Chromosome 22q11.2 Duplications. J Clin Immunol. 2023 05; 43(4):794-807.

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Mustillo PJ, Sullivan KE, Chinn IK, Notarangelo LD, Haddad E, Davies EG, de la Morena MT, Hartog N, Yu JE, Hernandez-Trujillo VP, Ip W, Franco J, Gambineri E, Hickey SE, Varga E, Markert ML. Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development. J Clin Immunol. 2023 02; 43(2):247-270.

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Crockett AM, Kebir H, Benallegue N, Adelman P, Gur RE, Sullivan K, Anderson SA, Alvarez JI. Immune status of the murine 22q11.2 deletion syndrome model. Eur J Immunol. 2023 01; 53(1):e2249840.

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Crowley TB, McGinn DM, Sullivan KE. 22q11.2 Deletion and Duplication Syndromes and COVID-19. J Clin Immunol. 2022 05; 42(4):746-748.

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Siper PM, Rowe MA, Guillory SB, Rouhandeh AA, George-Jones JL, Tavassoli T, Lurie S, Zweifach J, Weissman J, Foss-Feig J, Halpern D, Trelles MP, Mulhern MS, Brittenham C, Gordon J, Zemon V, Buxbaum JD, Kolevzon A. Visual Evoked Potential Abnormalities in Phelan-McDermid Syndrome. J Am Acad Child Adolesc Psychiatry. 2022 04; 61(4):565-574.e1.

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Abe K, Dowsett L, Wada R, Hutchins K. A pediatric case of acute myeloid leukemia with KMT2A gene rearrangement t(10;11) and 16p11.2 microdeletion syndrome. Pediatr Blood Cancer. 2021 02; 68(2):e28764.

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Deshpande DR, Demirdag YY, Marsh RA, Sullivan KE, Orange JS. Relationship Between Severity of T Cell Lymphopenia and Immune Dysregulation in Patients with DiGeorge Syndrome (22q11.2 Deletions and/or Related TBX1 Mutations): a USIDNET Study. J Clin Immunol. 2021 01; 41(1):29-37.

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Riel JM, Yamauchi Y, Ruthig VA, Malinta QU, Blanco M, Moretti C, Cocquet J, Ward MA. Rescue of Sly Expression Is Not Sufficient to Rescue Spermiogenic Phenotype of Mice with Deletions of Y Chromosome Long Arm. Genes (Basel). 2019 02 12; 10(2).

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Campbell IM, Sheppard SE, Crowley TB, McGinn DE, Bailey A, McGinn MJ, Unolt M, Homans JF, Chen EY, Salmons HI, Gaynor JW, Goldmuntz E, Jackson OA, Katz LE, Mascarenhas MR, Deeney VFX, Castelein RM, Zur KB, Elden L, Kallish S, Kolon TF, Hopkins SE, Chadehumbe MA, Lambert MP, Forbes BJ, Moldenhauer JS, Schindewolf EM, Solot CB, Moss EM, Gur RE, Sullivan KE, Emanuel BS, Zackai EH, McDonald-McGinn DM. What is new with 22q? An update from the 22q and You Center at the Children's Hospital of Philadelphia. Am J Med Genet A. 2018 10; 176(10):2058-2069.

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