National Center for Advancing and Translational Sciences Genetic and Rare Diseases Information Center, a program of the National Center for Advancing and Translational Sciences

Panhypopituitarism X-linked



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.

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Medical Terms Other Names
Learn More:
HPO ID
30%-79% of people have these symptoms
Abnormal prolactin level 0040086
Abnormality of secondary sexual hair 0009888
Amenorrhea
Abnormal absence of menstruation
0000141
Anterior pituitary hypoplasia
Underdeveloped pituitary gland
0010627
Aplasia/Hypoplasia of the breasts
Absent/small breasts
Absent/underdeveloped breasts
[ more ]
0010311
Decreased circulating ACTH level 0002920
Decreased testicular size
Small testes
Small testis
[ more ]
0008734
Depressed nasal ridge
Flat nose
Recessed nasal ridge
[ more ]
0000457
Fatigue
Tired
Tiredness
[ more ]
0012378
Hypoglycemia
Low blood sugar
0001943
Hypogonadotropic hypogonadism 0000044
Hypotension
Low blood pressure
0002615
Infertility 0000789
Pituitary hypothyroidism
Low thyroid gland function due to abnormal pituitary gland
0008245
5%-29% of people have these symptoms
Absence of secondary sex characteristics 0008187
Constipation 0002019
Delayed puberty
Delayed pubertal development
Delayed pubertal growth
Pubertal delay
[ more ]
0000823
Delayed skeletal maturation
Delayed bone maturation
Delayed skeletal development
[ more ]
0002750
Osteopenia 0000938
Osteoporosis of vertebrae 0005625
Pituitary dwarfism 0000839
1%-4% of people have these symptoms
Ectopic anterior pituitary gland 0012731
Ectopic posterior pituitary 0011755
Percent of people who have these symptoms is not available through HPO
Panhypopituitarism 0000871
X-linked inheritance 0001417
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Last updated: 7/1/2020

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.

Testing Resources

  • The Genetic Testing Registry (GTR) provides information about the genetic tests for this condition. The intended audience for the GTR is health care providers and researchers. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics 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.

Healthcare Resources


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.

Organizations Supporting this 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.

In-Depth Information

  • The Monarch Initiative brings together data about this condition from humans and other species to help physicians and biomedical researchers. Monarch’s tools are designed to make it easier to compare the signs and symptoms (phenotypes) of different diseases and discover common features. This initiative is a collaboration between several academic institutions across the world and is funded by the National Institutes of Health. Visit the website to explore the biology of this condition.
  • Online Mendelian Inheritance in Man (OMIM) is a catalog of human genes and genetic disorders. Each entry has a summary of related medical articles. It is meant for health care professionals and researchers. OMIM is maintained by Johns Hopkins University School of Medicine. 
  • Orphanet is a European reference portal for information on rare diseases and orphan drugs. Access to this database is free of charge.
  • PubMed is a searchable database of medical literature and lists journal articles that discuss Panhypopituitarism X-linked. Click on the link to view a sample search on this topic.

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.