FOXC2, forkhead box C2, 2303

N. diseases: 168; N. variants: 18
Disease: Hydrops Fetalis ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		0.320 GeneticVariation disease BEFREE From childhood onset lymphedema to fatal fetal hydrops: Possible modifying genes for a FOXC2 mutation. 30253460 2018
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		0.320 GeneticVariation disease BEFREE Mutations in the VEGFR3 and FOXC2 genes account for a subset of patients with unexplained in utero generalized subcutaneous edema and hydrops fetalis without family history of lymphedema. 19394045 2009
CUI: C0020305
Disease: Hydrops Fetalis
Hydrops Fetalis 		0.320 Biomarker disease GENOMICS_ENGLAND Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome. 11078474 2000