ORPHA:569821
Congenital primary lymphedema of Gordon
Also called VEGFC-related congenital primary lymphedema
- Body system
- Skin diseases
- Inheritance pattern
- Autosomal dominant
- Typical age of onset
- Adolescent, Adult, Childhood, Infancy, Neonatal
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:569821 is classified under "Skin diseases" in the Orphanet nomenclature.