Endocardial Fibroelastosis
"Endocardial Fibroelastosis" 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 condition characterized by the thickening of ENDOCARDIUM due to proliferation of fibrous and elastic tissue, usually in the left ventricle leading to impaired cardiac function (CARDIOMYOPATHY, RESTRICTIVE). It is most commonly seen in young children and rarely in adults. It is often associated with congenital heart anomalies (HEART DEFECTS CONGENITAL;) INFECTION; or gene mutation. Defects in the tafazzin protein, encoded by TAZ gene, result in a form of autosomal dominant familial endocardial fibroelastosis.
| Descriptor ID |
D004695
|
| MeSH Number(s) |
C14.280.238.281
|
| Concept/Terms |
Endocardial Fibroelastosis- Endocardial Fibroelastosis
- Endocardial Fibroelastoses
- Fibroelastoses, Endocardial
- Fibroelastosis, Endocardial
- Endomyocardial Fibroelastosis
|
Below are MeSH descriptors whose meaning is more general than "Endocardial Fibroelastosis".
Below are MeSH descriptors whose meaning is more specific than "Endocardial Fibroelastosis".
This graph shows the total number of publications written about "Endocardial Fibroelastosis" by people in UAMS Profiles by year, and whether "Endocardial Fibroelastosis" was a major or minor topic of these publications.
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Below are the most recent publications written about "Endocardial Fibroelastosis" by people in Profiles over the past ten years.