Is Kidney Disease Hereditary?

Rebekah Kuschmider
Rebekah Kuschmider
April 17, 2025
7
min read
Technically reviewed by: 
Charisse Cartin
Is Kidney Disease Hereditary?
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Kidney disease affects millions of people worldwide. Its causes can be linked to genetic factors. Understanding how family history and genetics play a role in the development of kidney disease can help you and your doctor set up the best plan for treating and monitoring your kidneys' health.

What Is Kidney Disease?

Kidney disease refers to any condition that compromises normal kidney functionWhen you have kidney failure, your kidneys can no longer filter waste products from your blood. This leads to dangerous levels of waste accumulating in your body.

The severity of kidney disease can vary. Some types can be managed with medication, dietary changes, and regular monitoring of kidney function. In more severe cases, dialysis or a kidney transplant may be necessary.

There are three main types of kidney disease:

  • Acute kidney injury is when your kidneys suddenly stop filtering wastes from the blood, which can happen within a few hours or daysThis condition is reversible.
  • Chronic kidney disease in children and adults is a lifelong condition that may grow more severe over time [3].
  • Hereditary kidney disease refers to kidney diseases that can be inherited. Congenital kidney disease develops before birth and can be hereditary [4].

Is Kidney Disease Hereditary?

Some kidney conditions develop due to genetic factors. Changes or mutations in certain genes or chromosomes can result in health conditions like kidney disease. Researchers have identified over 60 kidney diseases that are on the hereditary kidney disease listSome of the most common genetic kidney conditions include:

  • Autosomal dominant polycystic kidney disease (ADPKD): ADPKD is the most common inherited kidney disease. It causes benign cysts to develop in the kidneys. Symptoms usually start to develop in adulthood and include pain in the lower back and headaches [6].
  • Autosomal recessive polycystic kidney disease (ARPKD): ARPKD is a much rarer genetic disorder. ARPKD affects the liver and the kidneys, and symptoms are present from birth. It can cause kidney failure in children, along with liver function issues [7].
  • Fabry disease: Fabry disease occurs due to the absence of an enzyme that breaks down fats, carbohydrates, proteins, and other substances. The condition causes damage to the kidneys, as well as to the heart, eyes, ears, brain, and other organs [8].
  • Focal segmental glomerulosclerosis (FSGS): FSGS is caused by a genetic mutation that creates scarring on the tiny filters in your kidneys called the glomeruli. Damage to the glomeruli can lead to kidney failure [9].
  • Alport syndrome: Alport syndrome, also known as hereditary nephritis, causes kidney disease and other complications such as hearing and vision loss

Role of Genetics and Family History

Genetic disorders occur when one of your genes undergoes a change (known as a mutation or pathogenic variation) or when you have the wrong amount of genetic material [11].

Genes are passed on from parents to their children, with each parent contributing half of the child’s genetic makeup. Some genetic changes are dominant, which means having one gene with the mutation is enough to cause a disorder. In such cases, one parent can pass a condition to a child. Other changes are recessive, which means a child must inherit the affected gene from both parents to develop the condition.

Some genetic kidney diseases, such as ADPKD, are inherited from just one parent, while others, such as ARPKD, only develop when both parents pass the affected gene to their children.

Genetic kidney diseases can run in families, with some passed down from one parent and others requiring inherited changes from both.
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Genetic Testing for Early Detection

Genetic testing is available for many inheritable genetic disordersYou may ask for genetic testing to confirm a diagnosis if you’re experiencing symptoms of a genetic condition. In addition, couples can undergo carrier testing to determine if one or both prospective parents carry a mutation that could lead to genetic disorders in future children. This is especially important for couples with a family history of certain conditions.

Testing can reveal if you carry any genetic mutations, but it doesn’t mean you or your future children will develop a condition. A genetic counselor can explain your test results, any health risks to you or your children, and the steps you can take to protect your family’s health.

Using At-Home Urine Test Strips to Monitor Hereditary Kidney Disease

If you have an inherited kidney condition, you may need to conduct regular testing to evaluate your kidney function. Diagnox offers multiparameter urine test strips that you can use at home. These dipstick-style tests are easy to read and provide results in under 5 minutes. The Urinox-10 multiparameter urinalysis strips can test urine for:

The results of at-home urine tests can alert you to changes in your kidney health, which you can then discuss with your doctor.

Conclusion

Many types of kidney disease have genetic origins. Genetic testing can help diagnose symptomatic kidney disease and help families understand their risk of passing these conditions on to future children.

The symptoms and severity of kidney diseases can vary widely. Your doctor can explain your diagnosis and the best treatment options. Home testing to monitor kidney function can help you take control of your kidney health.

References

[1] Stanford Medicine Staff, “Kidney Failure,” Stanford Medicine, Availabe online [Accessed July 8, 2024].

[2] National Kidney Foundation Staff, “Acute Kidney Injury (AKI),” National Kidney Foundation, Available online [Accessed July 8, 2024].

[3] Mayo Clinic Staff, “Chronic kidney disease,” Mayo Clinic, Available online [Accessed July 8, 2024].

[4] UC Davis Health Staff, "Hereditary and Congenital Kidney Diseases," UC Davis Health, Available online[Accessed July 8, 2024].

[5] National Kidney Foundation Staff, “Inherited Kidney Disease,” National Kidney Foundation, Available online[Accessed July 8, 2024].

[6] M. Mahboob, P. Rout, S. W. Leslie, et al., "Autosomal Dominant Polycystic Kidney Disease,"[Updated 2024 Mar 20]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan[Accessed July 8, 2024].

[7] S. Subramanian, SW Leslie, T. Ahmad. "Autosomal Recessive Polycystic Kidney Disease. [Updated 2024 Mar 3]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan [Accessed July 8, 2024].

[8] SRA Bokhari, H. Zulfiqar, A. Hariz. "Fabry Disease," [Updated 2023 Jul 4]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan [Accessed July 8, 2024].

[9] Penn Medicine Staff, "Focal Segmental Glomerulosclerosis (FSGS)," Penn Medicine [Accessed July 8, 2024].

[10] Watson S, Padala SA, Hashmi MF, et al. "Alport Syndrome." [Updated 2023 Aug 14]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan [Accessed July 8, 2024].

[11] CDC Staff, “Genetic Disorders,” CDC [Accessed July 8, 2024].

[12] CDC Staff, “Genetic Testing,” CDC [Accessed July 8, 2024].

About the Author
Rebekah Kuschmider

Rebekah has been writing about culture, health, and politics since 2010. She has a masters degree in Arts Policy and Administration from The Ohio State University. Her work has been seen at WebMD, The Candidly, MedicineNet, YourTango, Ravishly, Babble, Scary Mommy, Salon, Role Reboot, The Good Men Project, SheSaid, Huffington Post, and Mamamia. She is a former cohost of the weekly podcast The More Perfect Union. Rebekah lives in Maryland with her husband, two kids, and a dog who sheds a lot.

About the Reviewer
This blog was
Technically reviewed by: 
Charisse Cartin

Charisse Cartin is a talented and dedicated editor who has contributed significantly to this blog.

The blog was also reviewed by the Diagnox content team. Diagnox Staff consists of a multidisciplinary team of scientists, content writers, and healthcare professionals with an expertise to create and review high-quality, informative, accurate, and easy-to-understand content for both professionals and everyday readers. Our staff follows strict guidelines to ensure the credibility and authenticity of the information, reviewing them independently and verifying them by various scientific and technical sources to ensure accuracy. Our review team believes in delivering knowledge free from bias to improve public health and well-being.

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