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GTR Home > Conditions/Phenotypes > Lymphatic malformation 11

Lymphatic malformation 11

Summary

Lymphatic malformation-11 (LMPHM11) is characterized by lower extremity edema, with onset in the second or third decade of life. Some affected individuals may have subclinical lymphatic malformations (Michelini et al., 2020). For a discussion of genetic heterogeneity of lymphatic malformation, see LMPHM1 (153100). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: JTK14, LMPHM11, TIE, TIE1
    Summary: tyrosine kinase with immunoglobulin like and EGF like domains 1

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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