ORPHA:79452
Milroy disease
Also called Hereditary lymphedema type I, Nonne-Milroy lymphedema
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Antenatal, Infancy, Neonatal
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:79452 is classified under "Skin diseases" in the Orphanet nomenclature.
Common signs
- Lymphedema
- Hydrocele testis
- Hyperkeratosis
- Ankle swelling
- Varicose veins
- Abnormal venous morphology