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||
|30%-79% of people have these symptoms|
|Abnormality of the dentition||
Dental abnormality[ more ]
|Aplasia/Hypoplasia of the eyebrow||
Absence of eyebrow
Lack of eyebrow
Missing eyebrow[ more ]
Cleft of the face
Central cleft upper lip
Decreased body height
Small stature[ more ]
|Sparse or absent eyelashes||0200102|
|Underdeveloped nasal alae||0000430|
|Upslanted palpebral fissure||
Upward slanting of the opening between the eyelids
|Wide nasal bridge||
Broad nasal bridge
Broad nasal root
Broadened nasal bridge
Increased breadth of bridge of nose
Increased breadth of nasal bridge
Increased width of bridge of nose
Increased width of nasal bridge
Nasal bridge broad
Wide bridge of nose
Widened nasal bridge[ more ]
|5%-29% of people have these symptoms|
|Abnormality of the humerus||0003063|
Inward turned thumb
|Aplasia/Hypoplasia affecting the eye||
Absent/underdeveloped eye[ more ]
|Camptodactyly of finger||0100490|
Abnormality of cognition
Mental impairment[ more ]
|Deep palmar crease||
Deep palm line
Little lower jaw
Small lower jaw[ more ]
|Percent of people who have these symptoms is not available through HPO|
|Abnormality of the skeletal system||
Skeletal anomalies[ more ]
|Cleft upper lip||
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.
If you need medical advice, you can look for doctors or other healthcare professionals who have experience with this disease. You may find these specialists through advocacy organizations, clinical trials, or articles published in medical journals. You may also want to contact a university or tertiary medical center in your area, because these centers tend to see more complex cases and have the latest technology and treatments.
If you can’t find a specialist in your local area, try contacting national or international specialists. They may be able to refer you to someone they know through conferences or research efforts. Some specialists may be willing to consult with you or your local doctors over the phone or by email if you can't travel to them for care.
You can find more tips in our guide, How to Find a Disease Specialist. We also encourage you to explore the rest of this page to find resources that can help you find specialists.
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.
Rare Disease Day at NIH on March 1, 2018
December 19, 2017
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