Structured Summary
Abstract
Emery-Dreifuss muscular dystrophy associated with mutations on LAMINS (LMNA gene).
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MeSH Record
Synonyms
12 entry terms
- Autosomal Emery Dreifuss Muscular Dystrophy
- Autosomal Dominant Emery-Dreifuss Muscular Dystrophy
- Emery-Dreifuss Muscular Dystrophy 2
- Emery-Dreifuss Muscular Dystrophy, Autosomal Dominant
- Hauptmann-Thannhauser Muscular Dystrophy
- Muscular Dystrophy With Early Contractures And Cardiomyopathy, Autosomal Dominant
- Muscular Dystrophy, Emery-Dreifuss, Autosomal Dominant
- Scapuloilioperoneal Atrophy with Cardiopathy
- Autosomal Dominant Emery Dreifuss Muscular Dystrophy
- Emery Dreifuss Muscular Dystrophy 2
- Emery Dreifuss Muscular Dystrophy, Autosomal Dominant
- Hauptmann Thannhauser Muscular Dystrophy
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
2021
MeSH Hierarchy
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AMA Style
References
- National Library of Medicine. Autosomal Emery-Dreifuss Muscular Dystrophy. Medical Subject Headings (MeSH). 2026. Unique ID D000083144. http://id.nlm.nih.gov/mesh/2026/D000083144
- Autosomal Emery-Dreifuss Muscular Dystrophy. In: Wikidata. https://www.wikidata.org/wiki/Q114753770