Structured Summary
Abstract
A congenital heart defect characterized by downward or apical displacement of the TRICUSPID VALVE, usually with the septal and posterior leaflets being attached to the wall of the RIGHT VENTRICLE. It is characterized by a huge RIGHT ATRIUM and a small and less effective right ventricle.
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Broader headings
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MeSH Record
Synonyms
12 entry terms
- Ebstein's Anomaly
- Ebstein's Malformation
- Anomaly, Ebstein
- Anomaly, Ebstein's
- Ebstein Malformation
- Ebsteins Anomaly
- Ebsteins Malformation
- Malformation, Ebstein's
- Familial Ebstein's Anomaly
- Ebstein's Anomaly, Familial
- Familial Ebstein Anomaly
- Familial Ebsteins Anomaly
MeSH Record
Aspects Covered
34 allowable subheadings
Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.
MeSH Record
History Note
2008 (1963)
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MeSH Record
NLM Classification
WG 220
AMA Style
References
- National Library of Medicine. Ebstein Anomaly. Medical Subject Headings (MeSH). 2026. Unique ID D004437. http://id.nlm.nih.gov/mesh/2026/D004437
- Ebstein Anomaly. In: Wikipedia. https://en.wikipedia.org/wiki/Ebstein%27s_anomaly
- Ebstein Anomaly. In: Wikidata. https://www.wikidata.org/wiki/Q277452