predominantly lower limb lymphedema Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Localized fluid retention and tissue swelling caused by a compromised lymphatic system, affecting mainly the legs. (Human Phenotype Ontology, HP_0003550)
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3 genes associated with the predominantly lower limb lymphedema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
FLT4 fms-related tyrosine kinase 4
FOXC2 forkhead box C2
SOX18 SRY (sex determining region Y)-box 18