MeSH Browser

MeSH Heading: Autosomal Emery-Dreifuss Muscular Dystrophy
Tree Number(s): C05.651.534.500.350.250; C10.668.491.175.500.350.250; C16.320.488.500; C16.320.577.350.250
Unique ID: D000083144
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D000083144
Scope Note: Emery-Dreifuss muscular dystrophy associated with mutations on LAMINS (LMNA gene).
Entry Term(s): 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
Public MeSH Note: 2021
History Note: 2021
Date Established: 2021/01/01
Date of Entry: 2020/07/07
Revision Date: 2020/02/28

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Autosomal Emery-Dreifuss Muscular Dystrophy MeSH Descriptor Data 2025