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Endocrinology / GeneticsHypoparathyroidismHypocalcemia

Hypoparathyroidism Panel

Analyzes 26 genes associated with inherited hypoparathyroidism to help identify genetic cause of parathyroid dysfunction and guide diagnostic evaluation.

Accessed through the DetectHypopara™ Sponsored Testing Program•Sponsored by Calcilytix Therapeutics•Performed by Prevention Genetics

Designed to help patients understand the purpose of testing and what to expect.

For patients

What this test and program do

This program provides no-cost genetic testing of 26 genes for U.S. or Canadian residents with non-surgical or idiopathic hypoparathyroidism, suspected genetic hypocalcemia, or a relative with genetic hypoparathyroidism.

Who this may help

Could this be right for you or your family?

  • Must reside in the United States or Canada.
  • May qualify with non-surgical hypoparathyroidism.
  • May qualify with idiopathic hypoparathyroidism.
  • May qualify with hypocalcemia suspected to be genetic in origin.
  • May qualify with a relative diagnosed with genetic hypoparathyroidism.
  • Testing must be ordered by a qualified health care provider.

What to expect

How the process works

  1. 1

    Confirm Eligibility

    Talk with your health care provider to see if you meet the program criteria and whether this hypoparathyroidism genetic test is appropriate.

  2. 2

    Provider Orders Test

    Your provider will order the test using the U.S. or Canada test requisition form and guide you on next steps for specimen collection.

  3. 3

    Provide a Specimen

    Your provider will collect your specimen and label it with at least two identifiers. Specimens are accepted Monday–Saturday; holiday schedules are posted in advance.

  4. 4

    Receive Your Results

    PreventionGenetics processes your sample, and results are typically sent to your provider about 18 days after all required materials are received.

Cost & coverage

Understanding potential costs

If you qualify for this program, the sponsor works with the laboratory to help make testing more affordable. Many patients pay little or no out-of-pocket cost. Your exact cost will depend on your insurance coverage and the specific criteria of the program, and the lab can explain what to expect before your sample is processed.

Quality & privacy

How your sample and information are handled

Testing is performed by Prevention Genetics, a CLIA-certified laboratory (CLIA 52D2065132) and College of American Pathologists (CAP) certified laboratory (CAP 7185561). Your sample is processed using validated methods and quality controls to support reliable genetic results.

Your health information is handled under privacy and security practices that are intended to align with applicable regulations. For program- and lab-specific details, review the privacy information provided by the laboratory and sponsor.

FAQ

Common questions about this program

What is this program?

This program provides no-cost genetic testing of 26 genes linked to hypoparathyroidism and genetic causes of hypocalcemia. Testing can help identify whether an inherited condition is contributing to your symptoms.

Who can receive testing?

You must live in the United States or Canada and have non-surgical hypoparathyroidism, idiopathic hypoparathyroidism, suspected genetic hypocalcemia, or a family history of genetic hypoparathyroidism. Testing must be ordered by a health care provider.

What does the genetic test look for?

The test analyzes genes involved in parathyroid gland development, PTH secretion, and inherited causes of hypocalcemia. Results may help clarify the underlying cause of your condition.

Is genetic counseling available?

Yes. Individuals tested through this program are eligible for no-charge post-test genetic counseling through Genome Medical, provided as part of the program.

How do I access genetic counseling?

Your provider can request counseling by:

• Completing and faxing the Genome Medical Genetic Counseling Referral Form, or

• Completing the post-test counseling section on the PreventionGenetics test requisition form.

Genome Medical will then contact you, usually within 24–48 hours, to schedule your session.

How long do results take?

Results are typically returned to your provider about 18 days after the specimen and required paperwork are received.

How do I get started?

Talk with your provider. They will confirm eligibility, order the test, collect your specimen, and review results with you.

Test details

  • ConditionsHypoparathyroidism, Hypocalcemia
  • Test typeTargeted NGS Panel
  • Test code15739
  • Genes / markers
    26
  • Key genes / markersCASR, GCM2, PTH, GATA3, CHD7
  • SpecimenWhole blood•Saliva•Buccal swab
  • Turnaround time2-3 Weeks
  • LabPrevention Genetics
  • Program regionUnited States, Canada

Next steps

Share this information with your endocrinologist or genetic specialist. They can help determine whether this test and program are appropriate for you.

Or ask your doctor to search for this test by name at Prevention Genetics.

Questions to ask your doctor about Hypoparathyroidism Panel

  1. Do you think this test is appropriate for me based on my symptoms and history?
  2. How could the results of this test change my diagnosis or treatment plan?
  3. What are the potential limitations of this test that I should understand?
  4. Should any of my family members also be tested based on my results?
  5. How will we follow up after the results are available?

Notes

See an issue with this program?

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