hereditary lymphedema I (Q60195052)

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hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood
  • Nonne-Milroy lymphedema
  • PCL
  • LMPH1
  • congenital primary lymphedema
  • Milroy disease
  • hereditary lymphedema type I
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Language Label Description Also known as
English
hereditary lymphedema I
hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood
  • Nonne-Milroy lymphedema
  • PCL
  • LMPH1
  • congenital primary lymphedema
  • Milroy disease
  • hereditary lymphedema type I

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