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Lynch Syndrome: Inherited Colorectal and Other Cancer Risk

A plain-language explainer on Lynch syndrome, an inherited condition that raises the risk of colorectal, endometrial, and some other cancers, and what it means for screening, based on National Cancer Institute genetics resources.

NCI source

Last reviewed: 2026-07-04

The short answer

Lynch syndrome is an inherited condition caused by changes in genes that normally help repair DNA. It raises the risk of colorectal cancer, endometrial (uterine) cancer, and some other cancers, often at younger ages. People with Lynch syndrome usually benefit from earlier and more frequent screening, guided by their care team.

  • Lynch syndrome is an inherited condition that raises the risk of several cancers.

  • It most often raises the risk of colorectal and endometrial (uterine) cancer.

  • Related cancers tend to appear at younger ages than usual.

  • It is caused by changes in genes that help repair DNA, passed down in families.

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The full explanation.

The simple version

Lynch syndrome is an inherited condition. It is caused by changes in genes that normally help your cells repair DNA. When those genes do not work well, errors can build up and raise the risk of certain cancers.

Lynch syndrome most often raises the risk of colorectal cancer (colon and rectum) and endometrial cancer (the lining of the uterus). It can raise the risk of some other cancers too, and related cancers often appear at younger ages than usual.

Lynch syndrome raises cancer risk — but knowing about it opens the door to screening that can catch or even prevent cancer.

How Lynch syndrome works

Your cells have a repair system that fixes small mistakes when DNA is copied, sometimes called mismatch repair. Lynch syndrome involves inherited changes in the genes that run this system.

When these genes do not work properly, mistakes in the DNA can pile up faster. Over time, that raises the chance that a cell will grow out of control and become cancer.

Because the change is inherited, it is present from birth and can be passed from a parent to a child.

Lynch syndrome makes the body's DNA "spell-check" less reliable, which raises cancer risk.

The cancers it affects

The two cancers most linked to Lynch syndrome are:

  • Colorectal cancer, cancer of the colon or rectum
  • Endometrial (uterine) cancer, cancer of the lining of the uterus

Lynch syndrome can also raise the risk of some other cancers, such as ovarian and stomach cancer, among others. A key feature is that these cancers often appear earlier in life than they would in the general population.

Signs it might run in your family

Cancer can appear in a family for many reasons, but certain patterns make an inherited condition like Lynch syndrome more likely. Talk with a doctor or genetic counselor if your family has:

  • Several relatives with colorectal or endometrial cancer
  • These cancers diagnosed at younger ages, such as colon cancer before 50
  • The same person having more than one related cancer
  • A combination of colon and endometrial cancer across close relatives

When possible, testing often starts with a relative who has had cancer, since that gives the clearest information for the whole family.

Early ages and repeating patterns of colon and uterine cancer are the classic red flags.

How it is found

Lynch syndrome is confirmed with genetic testing, usually from a blood or saliva sample, after a genetic counselor or doctor reviews your history.

Sometimes the path starts with the tumor. A person's cancer may be tested for features that suggest Lynch syndrome. If those features are present, inherited-risk testing follows to see whether the change was passed down.

A positive result means a higher risk of certain cancers — not that cancer is certain. Some people with Lynch syndrome never develop cancer.

What it means for screening

The biggest benefit of knowing you have Lynch syndrome is that it changes your screening plan. People with Lynch syndrome usually:

  • Start colorectal screening younger than average-risk adults
  • Screen more often, often with colonoscopy

Colonoscopy is especially valuable here because it can find and remove polyps before they become cancer, so screening can prevent cancer as well as catch it early.

Depending on the specific gene involved and personal history, screening or other steps for endometrial cancer and other related cancers may also be recommended.

For Lynch syndrome, earlier and more frequent screening is the main way to lower the danger.

Family and next steps

Because Lynch syndrome is inherited, a diagnosis carries information for your blood relatives. Siblings, children, and parents may share the same change and could benefit from testing and tailored screening.

A genetic counselor can help you understand your result, plan your own screening, and think through how to share the information with family. If Lynch syndrome runs in your family, your care team can build a screening schedule that fits your specific risk.

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Common questions

What is Lynch syndrome?

Lynch syndrome is an inherited condition caused by changes in genes that normally help repair DNA. These changes are passed down in families and raise the risk of certain cancers, especially colorectal and endometrial cancer. It is one of the more common inherited cancer conditions.

Which cancers does Lynch syndrome affect?

It most often raises the risk of colorectal (colon and rectal) cancer and endometrial (uterine) cancer. It can also raise the risk of some other cancers, such as ovarian, stomach, and certain others. Related cancers often appear at younger ages than usual.

How would I know if Lynch syndrome runs in my family?

Clues include several relatives with colorectal or endometrial cancer, cancers diagnosed at younger ages, or the same person having more than one related cancer. A doctor or genetic counselor can review your family history and see whether testing makes sense.

Does having Lynch syndrome mean I will get cancer?

No. It means your risk is higher than average, not that cancer is certain. Knowing you have it lets you and your care team use earlier and more frequent screening, which can catch cancer early or even prevent it by removing growths called polyps.

How is Lynch syndrome found?

It is confirmed with genetic testing, usually from a blood or saliva sample, after a review of your personal and family history. Sometimes a person's tumor is tested first for features that suggest Lynch syndrome, which then leads to inherited-risk testing.

What does screening look like for someone with Lynch syndrome?

It usually means starting colorectal screening, such as colonoscopy, at a younger age and repeating it more often than for people at average risk. Screening for other related cancers may also be recommended. Your care team will tailor a plan to you.

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  1. Q1.According to this article, what causes Lynch syndrome?
  2. Q2.According to this article, which two cancers are most linked to Lynch syndrome?
  3. Q3.According to this article, does having Lynch syndrome mean cancer is certain?
  4. Q4.According to this article, what is the main benefit of knowing you have Lynch syndrome?

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Lynch Syndrome: Inherited Colorectal and Other Cancer Risk