| Descriptor English: | Autosomal Emery-Dreifuss Muscular Dystrophy | ||||||
| Descriptor Spanish: |
Distrofia Muscular de Emery-Dreifuss Autosómica
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| Descriptor Portuguese: | Distrofia Muscular de Emery-Dreifuss Autossômica | ||||||
| Descriptor French: | Dystrophie musculaire d'Emery-Dreifuss autosomique | ||||||
| Entry term(s): |
Autosomal Dominant Emery Dreifuss Muscular Dystrophy Autosomal Dominant Emery-Dreifuss Muscular Dystrophy Autosomal Emery Dreifuss Muscular Dystrophy Emery Dreifuss Muscular Dystrophy 2 Emery Dreifuss Muscular Dystrophy, Autosomal Dominant Emery-Dreifuss Muscular Dystrophy 2 Emery-Dreifuss Muscular Dystrophy, Autosomal Dominant Hauptmann Thannhauser Muscular Dystrophy Hauptmann-Thannhauser Muscular Dystrophy Muscular Dystrophy With Early Contractures And Cardiomyopathy, Autosomal Dominant Muscular Dystrophy, Emery-Dreifuss, Autosomal Dominant Scapuloilioperoneal Atrophy with Cardiopathy |
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| 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 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000083144 | ||||||
| Scope note: | Emery-Dreifuss muscular dystrophy associated with mutations on LAMINS (LMNA gene). |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Public MeSH Note: | 2021 |
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| History Note: | 2021 |
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| DeCS ID: | 59371 | ||||||
| Unique ID: | D000083144 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2021/01/01 | ||||||
| Date of Entry: | 2020/07/07 | ||||||
| Revision Date: | 2020/02/28 |
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Autosomal Emery-Dreifuss Muscular Dystrophy
- Preferred
Autosomal Dominant Emery-Dreifuss Muscular Dystrophy
- Narrower
| Concept UI |
M000678757 |
| Scope note | Emery-Dreifuss muscular dystrophy associated with mutations on LAMINS (LMNA gene). |
| Preferred term | Autosomal Emery-Dreifuss Muscular Dystrophy |
| Entry term(s) |
Autosomal Emery Dreifuss Muscular Dystrophy |
| Concept UI |
M0464070 |
| Preferred term | Autosomal Dominant Emery-Dreifuss Muscular Dystrophy |
| Entry term(s) |
Autosomal Dominant Emery Dreifuss Muscular Dystrophy Emery Dreifuss Muscular Dystrophy 2 Emery Dreifuss Muscular Dystrophy, Autosomal Dominant Emery-Dreifuss Muscular Dystrophy 2 Emery-Dreifuss Muscular Dystrophy, Autosomal Dominant Hauptmann Thannhauser Muscular Dystrophy Hauptmann-Thannhauser Muscular Dystrophy Muscular Dystrophy With Early Contractures And Cardiomyopathy, Autosomal Dominant Muscular Dystrophy, Emery-Dreifuss, Autosomal Dominant Scapuloilioperoneal Atrophy with Cardiopathy |
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