Hemophilia C, also known as factor XI deficiency, is a rare bleeding disorder. Here are some key points:

- Cause: Most commonly caused by inheriting a mutated version of the F11 gene from both parents (autosomal recessive pattern). It can also be inherited from just one parent or caused by other conditions like systemic Show Full Answer

Hemophilia C, also known as factor XI deficiency, is a rare bleeding disorder. Here are some key points:

- Cause: Most commonly caused by inheriting a mutated version of the F11 gene from both parents (autosomal recessive pattern). It can also be inherited from just one parent or caused by other conditions like systemic lupus erythematosus (SLE) or Noonan syndrome.
- Symptoms: Symptoms can range from mild to moderate and include prolonged bleeding after surgery or injury.
- Inheritance: The risk of inheriting hemophilia C is the same for males and females.

For more detailed information, you can refer to the source: [What Is Hemophilia C? Symptoms, Treatment, and More | MyHemophiliaTeam](https://www.MyHemophiliaTeam.com/resources/what...).

 This AI-generated response comes from MyHemophiliaTeam and other selected sources. It is not a substitute for medical advice. Always ask your doctor about specific health concerns.

What Is Hemophilia C? Symptoms, Treatment, and More | MyHemophiliaTeam

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