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 | Learn More: HPO ID |
|---|---|---|
| 80%-99% of people have these symptoms | ||
| Myelofibrosis | 0011974 | |
| Pancytopenia |
Low blood cell count
|
0001876 |
| 30%-79% of people have these symptoms | ||
| Abnormality of bone marrow stromal |
0012129 | |
| Bone marrow hypercellularity | 0031020 | |
| Fatigue |
Tired
Tiredness
[ more ]
|
0012378 |
| Muscle weakness |
Muscular weakness
|
0001324 |
| 5%-29% of people have these symptoms | ||
| Acute myeloid leukemia | 0004808 | |
| Acute myelomonocytic leukemia | 0004820 | |
| Bone marrow hypocellularity |
Bone marrow failure
|
0005528 |
| Increased micromegakaryocyte count | 0031386 | |
| Low back pain | 0003419 | |
| Lymphocytosis |
High lymphocyte count
|
0100827 |
| Megakaryocyte |
0031385 | |
| 1%-4% of people have these symptoms | ||
| Splenomegaly |
Increased spleen size
|
0001744 |
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.
Living with a genetic or rare disease can impact the daily lives of patients and families. These resources can help families navigate various aspects of living with a rare disease.
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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