hereditary lymphedema Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A lymphedema commonly located_in legs, caused_by congenital abnormalities in the lymphatic system. (Human Disease Ontology, DOID_0050580)
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Genes

24 genes co-occuring with the disease hereditary lymphedema in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
FOXC2 forkhead box C2 2.31018
FLT4 fms-related tyrosine kinase 4 2.10376
VEGFC vascular endothelial growth factor C 1.67729
SOX18 SRY (sex determining region Y)-box 18 1.49964
ARAP3 ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3 1.43727
ITGA9 integrin, alpha 9 1.15837
PROX1 prospero homeobox 1 1.1072
FOXC1 forkhead box C1 1.04293
FIGF c-fos induced growth factor (vascular endothelial growth factor D) 0.805257
PTPN14 protein tyrosine phosphatase, non-receptor type 14 0.791721
EFNB2 ephrin-B2 0.729357
FOXO3 forkhead box O3 0.669538
PDPN podoplanin 0.630027
CCBE1 collagen and calcium binding EGF domains 1 0.625319
CANX calnexin 0.624535
FGFR4 fibroblast growth factor receptor 4 0.614356
FOXP2 forkhead box P2 0.60303
LYVE1 lymphatic vessel endothelial hyaluronan receptor 1 0.534248
GJC2 gap junction protein, gamma 2, 47kDa 0.446182
ANGPT2 angiopoietin 2 0.434524
ANGPT1 angiopoietin 1 0.393001
ATP7A ATPase, Cu++ transporting, alpha polypeptide 0.340906
PTPN11 protein tyrosine phosphatase, non-receptor type 11 0.214297
KDR kinase insert domain receptor 0.213621