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GTR Home > Conditions/Phenotypes > Lymphatic malformation 10

Summary

Lymphatic malformation-10 (LMPHM10) is an autosomal dominant disorder characterized by onset of lymphedema within the first year of life. Lymphedema primarily involves the lower extremities but may also occur in the neck, upper extremities, and scrotum or labia majora. Gradual resorption generally occurs, although some patients may experience progression complicated by cellulitis (Leppanen et al., 2020). For a discussion of genetic heterogeneity of lymphatic malformation, see 153100. [from OMIM]

Available tests

5 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: AGPT2, ANG2, LMPHM10, ANGPT2
    Summary: angiopoietin 2

Clinical features

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