National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Hereditary proximal myopathy with early respiratory failure



Other Names:
ADMERF; Edström Myopathy; Hereditary inclusion body myopathy with early respiratory failure; ADMERF; Edström Myopathy; Hereditary inclusion body myopathy with early respiratory failure; HMERF; HMERF-ERF; Myofibrillar myopathy with early respiratory failure; Myopathy, proximal, with early respiratory muscle involvement; HIBM-ERF; Hereditary myopathy with early respiratory failure; MFM-titinopathy; Myofibrillar myopathy-titinopathy See More
Categories:
This disease is grouped under:

This table lists symptoms that people with this disease may have. For most diseases, symptoms will vary from person to person. People with the same disease may not have all the symptoms listed. This information comes from a database called the Human Phenotype Ontology (HPO) . The HPO collects information on symptoms that have been described in medical resources. The HPO is updated regularly. Use the HPO ID to access more in-depth information about a symptom.

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Medical Terms Other Names
Learn More:
HPO ID
30%-79% of people have these symptoms
Elevated serum creatine kinase
Elevated blood creatine phosphokinase
Elevated circulating creatine phosphokinase
Elevated creatine kinase
Elevated serum CPK
Elevated serum creatine phosphokinase
High serum creatine kinase
Increased CPK
Increased creatine kinase
Increased creatine phosphokinase
Increased serum CK
Increased serum creatine kinase
Increased serum creatine phosphokinase
[ more ]
0003236
EMG: myopathic abnormalities 0003458
Foot dorsiflexor weakness
Foot drop
0009027
Increased variability in muscle fiber diameter 0003557
Internally nucleated skeletal muscle fibers 0031237
Limited hip movement 0008800
Muscle fiber splitting 0003555
Neck flexor weakness
Neck flexion weakness
0003722
Necrotizing myopathy 0008978
Orthopnea 0012764
Reduced vital capacity 0002792
Respiratory insufficiency due to muscle weakness
Decreased lung function due to weak breathing muscles
0002747
Restrictive ventilatory defect
Stiff lung or chest wall causing decreased lung volume
0002091
Rimmed vacuoles 0003805
Skeletal muscle atrophy
Muscle degeneration
Muscle wasting
[ more ]
0003202
Type 1 muscle fiber predominance 0003803
5%-29% of people have these symptoms
Calf muscle hypertrophy
Increased size of calf muscles
0008981
Muscle fiber hypertrophy 0100293
Proximal muscle weakness
Weakness in muscles of upper arms and upper legs
0003701
Tibialis muscle weakness 0008963
1%-4% of people have these symptoms
Falls 0002527
Percent of people who have these symptoms is not available through HPO
Adult onset
Symptoms begin in adulthood
0003581
Autosomal dominant inheritance 0000006
Diaphragmatic weakness
Weak diaphragm
0009113
Difficulty walking
Difficulty in walking
0002355
Frequent falls 0002359
Myofibrillar myopathy 0003715
Nocturnal hypoventilation 0002877
Pelvic girdle muscle weakness 0003749
Quadriceps muscle weakness
Quadriceps weakness
0003731
Respiratory failure 0002878
Shoulder girdle muscle weakness
Weak shoulder muscles
0003547
Slow progression
Signs and symptoms worsen slowly with time
0003677
Variable expressivity 0003828
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Last updated: 7/1/2020

If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease. You may find these specialists through advocacy organizations, clinical trials, or articles published in medical journals. You may also want to contact a university or tertiary medical center in your area, because these centers tend to see more complex cases and have the latest technology and treatments.

If you can’t find a specialist in your local area, try contacting national or international specialists. They may be able to refer you to someone they know through conferences or research efforts. Some specialists may be willing to consult with you or your local doctors over the phone or by email if you can't travel to them for care.

You can find more tips in our guide, How to Find a Disease Specialist. We also encourage you to explore the rest of this page to find resources that can help you find specialists.

Healthcare Resources


These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.

Where to Start

  • Genetics Home Reference (GHR) contains information on Hereditary proximal myopathy with early respiratory failure. This website is maintained by the National Library of Medicine.

In-Depth Information

  • GeneReviews provides current, expert-authored, peer-reviewed, full-text articles describing the application of genetic testing to the diagnosis, management, and genetic counseling of patients with specific inherited conditions.
  • The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
  • Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.

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