Orpha Number: 69085
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 | Learn More: HPO ID |
---|---|---|
30%-79% of people have these symptoms | ||
Absent lacrimal punctum | 0001092 | |
Absent nipple |
Absent nipples
|
0002561 |
Bilateral breast hypoplasia |
Two underdeveloped breasts
|
0012814 |
Breast aplasia |
Absent breast
|
0100783 |
Hypoplastic nipples |
Small nipples
|
0002557 |
Lacrimal duct atresia |
Unopened tear duct
|
0000564 |
5%-29% of people have these symptoms | ||
3-4 finger cutaneous |
0011939 | |
Bifid uvula | 0000193 | |
Blepharitis |
Inflammation of eyelids
|
0000498 |
Chronic irritative conjunctivitis | 0007717 | |
Cleft hard palate | 0410005 | |
0410030 | ||
Clinodactyly of the 5th finger |
Permanent curving of the pinkie finger
|
0004209 |
Dry skin | 0000958 | |
Hypodontia |
Failure of development of between one and six teeth
|
0000668 |
Hypohidrosis |
Decreased ability to sweat
Decreased sweating
Sweating, decreased
[ more ]
|
0000966 |
Nail dysplasia |
Atypical nail growth
|
0002164 |
Oligodactyly | 0012165 | |
Submucous cleft soft palate | 0011819 | |
Toe syndactyly |
Fused toes
Webbed toes
[ more ]
|
0001770 |
1%-4% of people have these symptoms | ||
Alopecia |
Hair loss
|
0001596 |
Aplasia of the ovary |
Absent ovary
|
0010463 |
Aplasia of the uterus |
Absent uterus
uterus absent
[ more ]
|
0000151 |
Freckling | 0001480 | |
Malar flattening |
Zygomatic flattening
|
0000272 |
Multiple cafe-au-lait spots | 0007565 | |
Primary amenorrhea | 0000786 | |
Protruding ear |
Prominent ear
Prominent ears
[ more ]
|
0000411 |
Psoriasiform dermatitis | 0003765 | |
Sparse eyebrow |
Sparse eyebrows
|
0045075 |
Percent of people who have these symptoms is not available through HPO | ||
0000006 | ||
Camptodactyly |
Permanent flexion of the finger or toe
|
0012385 |
Hallux valgus |
Bunion
|
0001822 |
Joint |
0009473 | |
Split foot |
Lobster-claw foot deformity
Split-foot
[ more ]
|
0001839 |
Split hand |
Claw hand
Claw hand deformities
Claw hands
Claw-hand deformities
Split-hand
[ more ]
|
0001171 |
Syndactyly |
Webbed fingers or toes
|
0001159 |
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.
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.