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|
|Percent of people who have these symptoms is not available through HPO|
|Abnormality of female external genitalia||
Abnormal female external genitalia
|Absence of secondary sex characteristics||0008187|
Increased body height
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
Is it possible for someone with Swyer syndrome to naturally start their period at a typical age (13)? See answer
Can women with Swyer syndrome experience orgasms? See answer
Is it possible for a patient with Swyer syndrome to get pregnant? If so, what methods should be used to ensure a successful pregnancy? See answer
I was born without ovaries. I have everything else that a normal woman has but I have streaks where ovaries would be. I was diagnosed when I was 15. My doctor put me on triphasil and soon after I started showing signs of puberty. None of my doctors seem to know about this condition. I am now 31. I am wondering if I should opt to have my streaks removed and if I should be on some other form of estrogen. I have very little breast development. See answer