KDR, kinase insert domain receptor, 3791

N. diseases: 623; N. variants: 23
Disease: HEMANGIOMA, CAPILLARY INFANTILE ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
HEMANGIOMA, CAPILLARY INFANTILE 		0.700 Biomarker disease GENOMICS_ENGLAND Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma. 18931684 2008
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
HEMANGIOMA, CAPILLARY INFANTILE 		0.700 GeneticVariation disease UNIPROT Suppressed NFAT-dependent VEGFR1 expression and constitutive VEGFR2 signaling in infantile hemangioma. 18931684 2008
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
HEMANGIOMA, CAPILLARY INFANTILE 		0.700 GeneticVariation disease UNIPROT Patterns of somatic mutation in human cancer genomes. 17344846 2007
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
HEMANGIOMA, CAPILLARY INFANTILE 		0.700 GeneticVariation disease UNIPROT Somatic mutation of vascular endothelial growth factor receptors in juvenile hemangioma. 11807987 2002
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
HEMANGIOMA, CAPILLARY INFANTILE 		0.700 Biomarker disease GENOMICS_ENGLAND
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
HEMANGIOMA, CAPILLARY INFANTILE 		0.700 Biomarker disease CTD_human
CUI: C1865871
Disease: HEMANGIOMA, CAPILLARY INFANTILE
HEMANGIOMA, CAPILLARY INFANTILE 		0.700 CausalMutation disease CLINVAR