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|
|Abnormality of macrophages||0004311|
|Abnormality of oral mucosa||
Abnormality of lining of mouth
|Abnormality of the nose||
Increased body temperature, episodic
Low blood cell count
Increased spleen size
|30%-79% of people have these symptoms|
|Elevated hepatic transaminases||
High liver enzymes
Low blood albumin
|5%-29% of people have these symptoms|
Decreased blood leukocyte number
Low platelet count
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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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