"Hirschsprung Disease" 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 MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON.
Descriptor ID |
D006627
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MeSH Number(s) |
C06.198.439 C06.405.469.158.701.439 C16.131.314.439
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Concept/Terms |
Hirschsprung Disease- Hirschsprung Disease
- Disease, Hirschsprung
- Megacolon, Congenital
- Hirschsprung's Disease
- Disease, Hirschsprung's
- Hirschsprungs Disease
- Megacolon, Aganglionic
- Aganglionic Megacolon
- Congenital Megacolon
Aganglionosis, Colonic- Aganglionosis, Colonic
- Colonic Aganglionosis
- Total Colonic Aganglionosis
- Aganglionosis, Total Colonic
|
Below are MeSH descriptors whose meaning is more general than "Hirschsprung Disease".
Below are MeSH descriptors whose meaning is more specific than "Hirschsprung Disease".
This graph shows the total number of publications written about "Hirschsprung Disease" by people in this website by year, and whether "Hirschsprung Disease" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1996 | 0 | 1 | 1 |
2011 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Hirschsprung Disease" by people in Profiles.
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Lower Gastrointestinal Functional and Motility Disorders in Children. Pediatr Clin North Am. 2021 12; 68(6):1255-1271.
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Robotic-assisted Soave procedure in an 18-year-old man with adult short-segment Hirschsprung's disease. Am Surg. 2013 Jun; 79(6):E223-5.
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Celiac disease and diabetes mellitus diagnosed in a pediatric patient with Hirschsprung disease. Fetal Pediatr Pathol. 2013 Feb; 31(1):7-12.
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Robotic Swenson pull-through for Hirschsprung's disease in infants. Am Surg. 2011 Jul; 77(7):937-41.
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The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis. JAMA. 1996 Nov 20; 276(19):1575-9.