FLT4, fms related receptor tyrosine kinase 4, 2324

N. diseases: 306; N. variants: 19
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0024236
Disease: Lymphedema
Lymphedema
0.330 GeneticVariation disease LHGDN Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease. 18279219 2008
CUI: C0024236
Disease: Lymphedema
Lymphedema
0.330 GeneticVariation disease LHGDN A novel VEGFR3 mutation causes Milroy disease. 17458866 2007
CUI: C0024236
Disease: Lymphedema
Lymphedema
0.330 AlteredExpression disease LHGDN Furthermore, mutations of vascular endothelial growth factor receptor 3 (VEGFR-3) have been observed in families with hereditary lymphedema. 15693535 2004
CUI: C0024236
Disease: Lymphedema
Lymphedema
0.330 Biomarker disease CTD_human