hereditary lymphedema I (Q60195052)
Jump to navigation
Jump to search
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
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 |
|
Statements
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference