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 fibula morphology||
Abnormality of the calf bone
|Aplasia/Hypoplasia of the tibia||
Absent/underdeveloped shinbone[ more ]
Decreased body height
Small stature[ more ]
|30%-79% of people have these symptoms|
|Aplasia/Hypoplasia of the thumb||
Absent/underdeveloped thumb[ more ]
|Synostosis of carpal bones||
Fusion of wrist bones
|Percent of people who have these symptoms is not available through HPO|
|Abnormal heart morphology||
Abnormality of the heart
Abnormally shaped heart[ more ]
Absent shinbone[ more ]
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.
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.
New NCATS Rare Diseases Research Video
December 27, 2017
Rare Disease Day at NIH on March 1, 2018
December 19, 2017
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