Term Name:	hereditary lymphedema I
Synonyms:	congenital primary lymphedema, hereditary lymphedema type I, LMPH1, Milroy disease, PCL
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.
Ontology:	Human Disease [DOID:0070212]   ( DOID:0070212 )