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 the
Failure of development of eyebrows
Failure of development of eyelashes
|Predominantly lower limb lymphedema||0003550|
|Sparse body hair||0002231|
|Sparse scalp hair||
Scalp hair, thinning
Sparse, thin scalp hair
sparse-absent scalp hair
|30%-79% of people have these symptoms|
Fullness of eyelids
Swelling of eyelids
|5%-29% of people have these symptoms|
|Percent of people who have these symptoms is not available through HPO|
|Abnormality of the dentition||
|Abnormality of the nail||0001597|
|Nonimmune hydrops fetalis||0001790|
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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