Q82: Other congenital malformations of skin
Q82.0: Hereditary lymphoedema
Hereditary lymphedema is a genetic condition that involves swelling (edema) due to an impaired lymphatic system, which plays a crucial role in your immune function and fluid balance. In people with this condition, the body has trouble clearing away waste materials and immune cells from tissues, leading to localized or widespread swelling, most often in the arms or legs. Symptoms usually become apparent at birth or during puberty when hormonal changes can trigger the onset. The primary indication is noticeable swelling, which can impact daily activities and quality of life. As a hereditary condition, it is passed on within families, typically through an abnormal gene you receive from one or both parents. The disease progression varies, meaning some individuals will have mild swelling and others will have a more extreme presentation. Regardless of the severity, it is a chronic condition and requires lifelong management.
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The information provided on this page is for general educational purposes only. It is not intended for self-diagnosis and does not replace professional medical advice. Always consult your doctor or a qualified healthcare provider with any questions or concerns about your health.
If you see an ICD diagnosis code (e.g., on a medical report), be aware that doctors may also include additional indicators to express diagnostic certainty. Only a healthcare professional can interpret these codes accurately in the context of your individual case.
For a complete understanding of your condition and what the diagnosis means for you, please speak directly with your doctor.