nonimmune hydrops fetalis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of hydrops fetalis in which there is no identifiable circulating antibody to red blood cell antigens . (Human Phenotype Ontology, HP_0001790)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001790
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Genes

9 genes associated with the nonimmune hydrops fetalis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALG1 ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase
COL1A1 collagen, type I, alpha 1
COL1A2 collagen, type I, alpha 2
FLT4 fms-related tyrosine kinase 4
GBA glucosidase, beta, acid
LBR lamin B receptor
PKLR pyruvate kinase, liver and RBC
PMM2 phosphomannomutase 2
SOX18 SRY (sex determining region Y)-box 18