22q11 Deletion Syndrome

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22q11 Deletion Syndrome

"22q11 Deletion Syndrome" 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

Condition with a variable constellation of phenotypes due to deletion polymorphisms at chromosome location 22q11. It encompasses several syndromes with overlapping abnormalities including the DIGEORGE SYNDROME, VELOCARDIOFACIAL SYNDROME, and CONOTRUNCAL AMOMALY FACE SYNDROME. In addition, variable developmental problems and schizoid features are also associated with this syndrome. (From BMC Med Genet. 2009 Feb 25;10:16) Not all deletions at 22q11 result in the 22q11deletion syndrome.

Descriptor ID	D058165
MeSH Number(s)	C05.660.207.103 C14.240.400.021 C14.280.400.044 C15.604.451.249 C16.131.077.019 C16.131.240.400.021 C16.131.260.019 C16.131.482.249 C16.131.621.207.103 C16.320.180.019 C19.642.482.500
Concept/Terms	22q11 Deletion Syndrome 22q11 Deletion Syndrome 22q11 Deletion Syndromes Deletion Syndrome, 22q11 Deletion Syndromes, 22q11 Syndrome, 22q11 Deletion Syndromes, 22q11 Deletion

Below are MeSH descriptors whose meaning is more general than "22q11 Deletion Syndrome".

Diseases [C]
Musculoskeletal Diseases [C05]
Musculoskeletal Abnormalities [C05.660]
Craniofacial Abnormalities [C05.660.207]
22q11 Deletion Syndrome [C05.660.207.103]
Cardiovascular Diseases [C14]
Cardiovascular Abnormalities [C14.240]
Heart Defects, Congenital [C14.240.400]
22q11 Deletion Syndrome [C14.240.400.021]
Heart Diseases [C14.280]
Heart Defects, Congenital [C14.280.400]
22q11 Deletion Syndrome [C14.280.400.044]
Hemic and Lymphatic Diseases [C15]
Lymphatic Diseases [C15.604]
Lymphatic Abnormalities [C15.604.451]
22q11 Deletion Syndrome [C15.604.451.249]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
Congenital Abnormalities [C16.131]
Abnormalities, Multiple [C16.131.077]
22q11 Deletion Syndrome [C16.131.077.019]
Cardiovascular Abnormalities [C16.131.240]
Heart Defects, Congenital [C16.131.240.400]
22q11 Deletion Syndrome [C16.131.240.400.021]
Chromosome Disorders [C16.131.260]
22q11 Deletion Syndrome [C16.131.260.019]
Lymphatic Abnormalities [C16.131.482]
22q11 Deletion Syndrome [C16.131.482.249]
Musculoskeletal Abnormalities [C16.131.621]
Craniofacial Abnormalities [C16.131.621.207]
22q11 Deletion Syndrome [C16.131.621.207.103]
Genetic Diseases, Inborn [C16.320]
Chromosome Disorders [C16.320.180]
22q11 Deletion Syndrome [C16.320.180.019]
Endocrine System Diseases [C19]
Parathyroid Diseases [C19.642]
Hypoparathyroidism [C19.642.482]
22q11 Deletion Syndrome [C19.642.482.500]

Below are MeSH descriptors whose meaning is related to "22q11 Deletion Syndrome".

Below are MeSH descriptors whose meaning is more specific than "22q11 Deletion Syndrome".

22q11 Deletion Syndrome
DiGeorge Syndrome

publications

Timeline | Most Recent

This graph shows the total number of publications written about "22q11 Deletion Syndrome" by people in UAMS Profiles by year, and whether "22q11 Deletion Syndrome" was a major or minor topic of these publications.

Bar chart showing 3 publications over 3 distinct years, with a maximum of 1 publications in 2010 and 2012 and 2015

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

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