Orpha Number: 3144
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|
Short limb dwarfism, disproportionate
Short-limbed dwarfism[ more ]
Short calf bone
Small shoulder blade
|Hypoplastic vertebral bodies||0008479|
|Increased fibular diameter||
Wide calf bone
|Lateral clavicle hook||
Increased size of skull
Large head circumference[ more ]
Low chest circumference
Narrow shoulders[ more ]
Decreased length of neck
|30%-79% of people have these symptoms|
|Abnormality of the fingernails||
Undescended testis[ more ]
|5%-29% of people have these symptoms|
|Accelerated skeletal maturation||0005616|
|Advanced tarsal ossification||0008108|
|Dumbbell-shaped long bone||0000947|
|Percent of people who have these symptoms is not available through HPO|
|Advanced ossification of carpal bones||0004233|
|Anterior rib cupping||0000907|
|Flat acetabular roof||0003180|
Irregular wide portion of a long bone
Decreased size of midface
Underdevelopment of midface[ more ]
|Ovoid vertebral bodies||0003300|
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.
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.