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|
|Abnormal cortical bone morphology||0003103|
|Abnormal enchondral ossification||0003336|
|Abnormal form of the vertebral bodies||0003312|
|Abnormality of the intervertebral disk||0005108|
|Abnormality of the metaphysis||
Abnormality of the wide portion of a long bone
|Abnormality of the ribs||
|Depressed nasal bridge||
Depressed bridge of nose
Flat bridge of nose
Flat nasal bridge
Flat, nasal bridge
Flattened nasal bridge
Low nasal bridge
Low nasal root[ more ]
|Hypoplastic cervical vertebrae||0008434|
Stiff joints[ more ]
Round back[ more ]
Long rib cage
Low chest circumference
Narrow shoulders[ more ]
|Rough bone trabeculation||0100670|
|Severe short stature||
Short stature, severe[ more ]
|5%-29% of people have these symptoms|
|Aplasia/Hypoplasia of the lungs||
Absent/underdeveloped lungs[ more ]
|Camptodactyly of finger||0100490|
|Clinodactyly of the 5th finger||0004209|
|Fetal akinesia sequence||0001989|
|Low-set, posteriorly rotated ears||0000368|
|Peripheral axonal neuropathy||0003477|
|Percent of people who have these symptoms is not available through HPO|
|Abnormal metaphyseal vascular invasion||0003562|
|Absent primary metaphyseal spongiosa||0003332|
Dumbbell shaped wide portion of long bone
|Flared femoral metaphysis||0002834|
|Flared humeral metaphysis||
Flared wide portion of long bone of upper arm
|Hyperplasia of the femoral trochanters||0002822|
|Relatively short spine||0002766|
Stubby fingers[ more ]
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.
Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.
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.
Got a Great Research Idea? ‘All of Us’ Wants to Hear It!
January 18, 2018
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. Submit a new question
I was diagnosed with a rare disease as a child. Recently, at age 21, I learned that I have metatropic dwarfism (also known as metatropic dysplasia). My doctors haven't been able to give me much information. Can you tell me more about this condition, including treatment options? See answer