Autosomal Emery-Dreifuss Muscular Dystrophy

Emery-Dreifuss muscular dystrophy associated with mutations on LAMINS (LMNA gene).

Also Known As:

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; Autosomal Emery Dreifuss Muscular Dystrophy; Emery Dreifuss Muscular Dystrophy 2; Emery Dreifuss Muscular Dystrophy, Autosomal Dominant; Hauptmann Thannhauser Muscular Dystrophy

Musculoskeletal Diseases: 719
- Muscular Diseases: 10128
  - Atrophic Muscular Disorders: 320
    - Muscular Dystrophies: 5779
      - Emery-Dreifuss Muscular Dystrophy: 288
        Autosomal Emery-Dreifuss Muscular Dystrophy: 44
Nervous System Diseases: 14178
- Neuromuscular Diseases: 2005
  - Muscular Diseases: 10128
    - Atrophic Muscular Disorders: 320
      - Muscular Dystrophies: 5779
        Emery-Dreifuss Muscular Dystrophy: 288
        Autosomal Emery-Dreifuss Muscular Dystrophy: 44
Congenital, Hereditary, and Neonatal Diseases and Abnormalities: 933
- Inborn Genetic Diseases: 11939
  - Muscular Dystrophies: 5779
    - Emery-Dreifuss Muscular Dystrophy: 288
      - Autosomal Emery-Dreifuss Muscular Dystrophy: 44
  - Laminopathies: 484
    - Autosomal Emery-Dreifuss Muscular Dystrophy: 44

Anne-Mari Håkelien Selected Research

Anne-Mari Håkelien Research Topics

Disease

Drug/Important Bio-Agent (IBA)