hereditary lymphedema I
ORPHA: 79452
Overview
hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with hereditary lymphedema I, sourced from HPO and Orphanet clinical annotations.
LymphedemaHydrocele testisHyperkeratosisAnkle swellingVaricose veinsAbnormal venous morphologyPredominantly lower limb lymphedemaPedal edemaCellulitisToenail dysplasiaEpicanthusAtypical behaviorSpecific learning disabilityNeoplasm of the skinLichenificationAngiosarcomaErysipelasAbnormal facial shape
Classification & Codes
Orphanet Code
ORPHA:79452hereditary lymphedema I
| Orphanet | ORPHA:79452 |
| Treatments | 0 drug(s) |
| Symptoms on record | 18 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO