 Heterotaxy Syndrome
"Heterotaxy 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.
Abnormal thoracoabdominal VISCERA arrangement (visceral heterotaxy) or malformation that involves additional CONGENITAL HEART DEFECTS (e.g., heart isomerism; DEXTROCARDIA) and/or abnormal SPLEEN (e.g., asplenia and polysplenia). Irregularities with the central nervous system, the skeleton and urinary tract are often associated with the syndrome.
| Descriptor ID |
D059446
|
| MeSH Number(s) |
C14.240.400.592 C14.280.400.592 C15.604.744.146 C16.131.077.401 C16.131.240.400.592
|
| Concept/Terms |
Heterotaxy Syndrome- Heterotaxy Syndrome
- Heterotaxy Syndromes
- Syndrome, Heterotaxy
- Syndromes, Heterotaxy
Visceral Heterotaxy- Visceral Heterotaxy
- Heterotaxies, Visceral
- Heterotaxy, Visceral
- Visceral Heterotaxies
- Situs Ambiguus Viscerum
- Ambiguus Viscerum, Situs
- Ambiguus Viscerums, Situs
- Situs Ambiguus Viscerums
- Viscerum, Situs Ambiguus
- Viscerums, Situs Ambiguus
- Situs Ambiguus
- Ambiguus, Situs
Polysplenia Syndrome- Polysplenia Syndrome
- Polysplenia Syndromes
- Syndrome, Polysplenia
- Syndromes, Polysplenia
- Situs Ambiguus with Polysplenia
- Left Atrial Isomerism with Polysplenia
Right Atrial Isomerism- Right Atrial Isomerism
- Atrial Isomerism, Right
- Atrial Isomerisms, Right
- Isomerism, Right Atrial
- Isomerisms, Right Atrial
- Right Atrial Isomerisms
Asplenia Syndrome- Asplenia Syndrome
- Asplenia Syndromes
- Syndrome, Asplenia
- Syndromes, Asplenia
- Situs Ambiguus with Asplenia
- Right Atrial Isomerism with Asplenia
- Asplenia with Cardiovascular Anomalies
- Ivemark Syndrome
- Syndrome, Ivemark
Left Atrial Isomerism- Left Atrial Isomerism
- Atrial Isomerism, Left
- Atrial Isomerisms, Left
- Isomerism, Left Atrial
- Isomerisms, Left Atrial
- Left Atrial Isomerisms
|
Below are MeSH descriptors whose meaning is more general than "Heterotaxy Syndrome".
Below are MeSH descriptors whose meaning is more specific than "Heterotaxy Syndrome".
This graph shows the total number of publications written about "Heterotaxy Syndrome" by people in this website by year, and whether "Heterotaxy Syndrome" 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 |
|---|
| 2015 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Heterotaxy Syndrome" by people in Profiles.
-
Guimier A, Gabriel GC, Bajolle F, Tsang M, Liu H, Noll A, Schwartz M, El Malti R, Smith LD, Klena NT, Jimenez G, Miller NA, Oufadem M, Moreau de Bellaing A, Yagi H, Saunders CJ, Baker CN, Di Filippo S, Peterson KA, Thiffault I, Bole-Feysot C, Cooley LD, Farrow EG, Masson C, Schoen P, Deleuze JF, Nitschk? P, Lyonnet S, de Pontual L, Murray SA, Bonnet D, Kingsmore SF, Amiel J, Bouvagnet P, Lo CW, Gordon CT. MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates. Nat Genet. 2015 Nov; 47(11):1260-3.
|
People  People who have written about this concept. _
Similar Concepts
People who have written about this concept.
_
Top Journals
Top journals in which articles about this concept have been published.
|