predominantly lower limb lymphedema Gene Set

Dataset GWASdb SNP-Phenotype 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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5 genes associated with the predominantly lower limb lymphedema phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1 0.911279
ITFG1 integrin alpha FG-GAP repeat containing 1 0.846153
DLG2 discs, large homolog 2 (Drosophila) 0.837193
HNF1B HNF1 homeobox B 0.754763
FILIP1L filamin A interacting protein 1-like 0.620705