hereditary lymphedema I (DOID:0070212)
Alliance: disease page
Synonyms: congenital primary lymphedema; hereditary lymphedema type I; LMPH1; Milroy disease; Nonne-Milroy lymphedema; PCL
Alt IDs: ICD10CM:Q82.0, MESH:D008209, NCI:C48829, ORDO:79452, UMLS_CUI:C1704423
Definition: A hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood.