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|
|Delayed onset bleeding||0040232|
Blood in urine
Bleeding within the skull
Bleeding within a joint
|Poor wound healing||0001058|
|Prolonged bleeding after dental extraction||0006298|
|Prolonged bleeding after surgery||
Excessive bleeding during surgery
Protracted bleeding after surgery
|Prolonged bleeding time||0003010|
|Prolonged partial thromboplastin time||0003645|
|Reduced factor IX activity||0011858|
|Spontaneous, recurrent epistaxis||
Spontaneous, recurrent nosebleed
|Percent of people who have these symptoms is not available through HPO|
Degenerative joint disease
|Persistent bleeding after trauma||
Excessive bleeding after minor trauma
Frequent bleeding with trauma
Prolonged bleeding after minor trauma
|Prolonged whole-blood clotting time||0005542|
The resources below provide information about treatment options for this condition. If you have questions about which treatment is right for you, talk to your healthcare professional.
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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.
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.
World Federation of Hemophilia
July 19, 2016
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