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.
|Medical Terms||Other Names||
|80%-99% of people have these symptoms|
|Progressive distal muscle weakness||0009063|
|30%-79% of people have these symptoms|
|Functional motor deficit||0004302|
|Limb muscle weakness||
|Limited wrist extension||0006251|
|Motor conduction block||0012078|
|Progressive muscle weakness||0003323|
|Reduced tendon reflexes||0001315|
|Weakness of long finger extensor muscles||0009077|
Research helps us better understand diseases and can lead to advances in diagnosis and treatment. This section provides resources to help you learn about medical research and ways to get involved.
Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.
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.
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Is multifocal motor neuropathy hereditary? We have no family history that I know of. My son was diagnosed with MMN at age 29, if he has children are they at risk? See answer