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Start free with EleplanMeige disease
ORPHA:90186Disease
Also called Hereditary lymphedema type II · Meige lymphedema
What it is
Meige disease is a frequent form of late-onset, primary lymphedema characterized by lower limb lymphedema typically developing during puberty.
Key facts
- Age of onset
- Adolescent, Childhood
- Inheritance
- Not applicable
- Classified as
- Disease
Signs and symptoms
Common30–79%
11Sometimes5–29%
9- Angiosarcoma
- Edema of the dorsum of hands
- Facial edema
- Laryngeal edema
- Periorbital edema
- Peripheral edema
- Pleural effusion
- Skin ulcer
and 1 more in this range
These ranges are how often a sign appears across everyone diagnosed, not a prediction for one person — most people have some of these and not others. Orphanet also records findings that are specifically absent in this disease; those are in the data but not listed here.
Gene
ICD-10 codes
ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.
Related health topics
Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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