FOXP3, forkhead box P3, 50943

N. diseases: 688; N. variants: 27
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 		0.300 Biomarker disease GENOMICS_ENGLAND Identification of a novel nonsense mutation in the FOXP3 gene in a fetus with hydrops--Expanding the phenotype of IPEX syndrome. 26395338 2016