"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 |
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2001 | 0 | 1 | 1 |
2011 | 0 | 1 | 1 |
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Below are the most recent publications written about "Abnormalities, Multiple" by people in Profiles.
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Asymmetric phenotype of Axenfeld-Rieger anomaly and aniridia associated with a novel PITX2 mutation. Mol Vis. 2011; 17:1231-8.
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Serial sonographic findings in a fetus with congenital hiatal hernia. Ultrasound Obstet Gynecol. 2001 Apr; 17(4):350-3.
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Candidate region for Coffin-Siris syndrome at 7q32-->34. Am J Med Genet. 2000 Jul 31; 93(3):241-3.
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Exstrophy of the cloaca in a 47,XXX child: review of genitourinary malformations in triple-X patients. Am J Med Genet. 1993 Mar 15; 45(6):761-3.