"Hernia, Umbilical" 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.
A HERNIA due to an imperfect closure or weakness of the umbilical ring. It appears as a skin-covered protrusion at the UMBILICUS during crying, coughing, or straining. The hernia generally consists of OMENTUM or SMALL INTESTINE. The vast majority of umbilical hernias are congenital but can be acquired due to severe abdominal distention.
| Descriptor ID |
D006554
|
| MeSH Number(s) |
C16.614.378 C23.300.707.374.937.500
|
| Concept/Terms |
Hernia, Umbilical- Hernia, Umbilical
- Exomphalos
- Umbilical Hernia
- Hernias, Umbilical
- Umbilical Hernias
|
Below are MeSH descriptors whose meaning is more general than "Hernia, Umbilical".
- Diseases [C]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Infant, Newborn, Diseases [C16.614]
- Hernia, Umbilical [C16.614.378]
- Pathological Conditions, Signs and Symptoms [C23]
- Pathological Conditions, Anatomical [C23.300]
- Hernia [C23.300.707]
- Hernia, Abdominal [C23.300.707.374]
- Hernia, Ventral [C23.300.707.374.937]
- Hernia, Umbilical [C23.300.707.374.937.500]
Below are MeSH descriptors whose meaning is more specific than "Hernia, Umbilical".
This graph shows the total number of publications written about "Hernia, Umbilical" by people in this website by year, and whether "Hernia, Umbilical" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1995 | 1 | 0 | 1 |
| 2012 | 1 | 0 | 1 |
| 2013 | 1 | 0 | 1 |
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Below are the most recent publications written about "Hernia, Umbilical" by people in Profiles.
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Maternal reporting of prenatal ultrasounds among women in the National Birth Defects Prevention Study. Birth Defects Res A Clin Mol Teratol. 2014 Jan; 100(1):4-12.
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Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. J Med Genet. 2012 Apr; 49(4):270-6.
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Abdominal wall defects in infants. Survival and implications for adult life. Ann Surg. 1995 May; 221(5):525-8; discussion 528-30.