Orpha Number: 156728
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|
|Bowing of the legs||
Bowed lower limbs[ more ]
Short limbs[ more ]
|30%-79% of people have these symptoms|
Short limb dwarfism, disproportionate
Short-limbed dwarfism[ more ]
|Limited elbow extension||
Decreased elbow extension
Elbow limited extension
Limitation of elbow extension
Limited extension at elbows
Limited forearm extension
Restricted elbow extension[ more ]
Waddling walk[ more ]
|5%-29% of people have these symptoms|
Flat facial shape
Small thorax[ more ]
|Percent of people who have these symptoms is not available through HPO|
|Dysplastic iliac wings||0008794|
|Flat acetabular roof||0003180|
|Hypoplastic pubic bone||0003173|
Irregular end part of long bone
Broad wide portion of long bone
|Narrow iliac wings||0002868|
|Ovoid vertebral bodies||0003300|
|Posterior rib cupping||0000922|
|Short long bone||
Long bone shortening
Small end part of bone
Making a diagnosis for a genetic or rare disease can often be challenging. Healthcare professionals typically look at a person’s medical history, symptoms, physical exam, and laboratory test results in order to make a diagnosis. The following resources provide information relating to diagnosis and testing for this condition. If you have questions about getting a diagnosis, you should contact a healthcare professional.
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
Questions sent to GARD may be posted here if the information could be helpful to others. We remove all identifying information when posting a question to protect your privacy. If you do not want your question posted, please let us know.