MeSH Browser

MeSH Heading: X-Linked Emery-Dreifuss Muscular Dystrophy
Tree Number(s): C05.651.534.500.350.500; C10.668.491.175.500.350.500; C16.320.322.625.500; C16.320.577.350.500
Unique ID: D000083143
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D000083143
Scope Note: Emery-Dreifuss muscular dystrophy associated with mutations on emerin (EMD gene) or four and a half LIM domains 1 (FHL1 gene) both located on X chromosome.
Entry Term(s): Benign Scapuloperoneal Muscular Dystrophy with Early Contractures; EDMD1; Emerinopathy; Emery-Dreifuss Muscular Dystrophy 1; Emery-Dreifuss Muscular Dystrophy 1, X-Linked; Emery-Dreifuss Muscular Dystrophy 6; Emery-Dreifuss Muscular Dystrophy 6, X-Linked; Emery-Dreifuss Muscular Dystrophy, 1; Emery-Dreifuss Muscular Dystrophy, X-Linked; Muscular Dystrophy, Emery-Dreifuss, X-Linked; Myopathy, X-Linked, With Postural Muscle Atrophy; Scapuloperoneal Syndrome, X-Linked; XMPMA
Public MeSH Note: 2021
History Note: 2021
Date Established: 2021/01/01
Date of Entry: 2020/07/07
Revision Date: 2021/05/10

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)

X-Linked Emery-Dreifuss Muscular Dystrophy MeSH Descriptor Data 2023