Genetic mutation screening for dysgenetic (developmental) kidney disease panel (whole blood)
This test checks for genetic changes that may affect how your kidneys develop. It’s used if you or your doctor suspect a condition called dysgenetic kidney disease, which can cause problems with kidney formation before birth.
["Helps identify genetic risks for kidney development issues that may require early medical attention."]
Key facts at a glance
- LOINC
- 43745-9
- Short code
- DYS gene Mut Tested Bld/T
- Synonyms
- DYS gene Mut Tested Bld/T
- Category
- chemistry
- Sample
- whole-blood
- Container
- Lavender-top (EDTA)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- molgen
- Specimen volume
- 3 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h
- Hemolysis max
- 0
- Lipemia max
- 0
- Icterus max
- 0
- TAT
- 4–24 hours
- Order
- routine
Why This Test Might Be Ordered
Your doctor may recommend this test if you have a family history of kidney problems, birth defects involving the kidneys, or if you’ve been diagnosed with a condition like renal dysplasia or other congenital kidney abnormalities. It’s also sometimes used in prenatal screening or if you’re considering genetic counseling.
What to Expect Before the Test
You’ll provide a small sample of whole blood, usually drawn from your arm. This is similar to a regular blood draw. No special preparation is needed, but tell your doctor about any medications or health conditions you have before the test.
What the Results Mean
The test looks for specific genetic mutations linked to kidney development issues. If mutations are found, they may explain why you or your child has kidney problems. Results can help guide treatment plans, such as monitoring, surgery, or specialized care.
Common Conditions This Test Helps Diagnose
This screening can help diagnose conditions like renal dysplasia (underdeveloped kidneys), renal agenesis (missing kidneys), or other structural kidney abnormalities caused by genetic mutations.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
◆Associated findings1
Short name
Kidney Development Mutation Screen
Frequently asked questions
How often will I need this test?
What if my test results are positive?
Can this test be done during pregnancy?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy