Persistent Fetal Circulation Syndrome Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_13042)
External Link	https://www.disgenet.org/browser/0/1/0/C0031190
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Genes

11 genes associated with the disease Persistent Fetal Circulation Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
ABCA3	ATP-binding cassette, sub-family A (ABC1), member 3
CPS1	carbamoyl-phosphate synthase 1, mitochondrial
ESRP1	epithelial splicing regulatory protein 1
FOXF1	forkhead box F1
NOS3	nitric oxide synthase 3 (endothelial cell)
OLA1	Obg-like ATPase 1
PTEN	phosphatase and tensin homolog
SIRPA	signal-regulatory protein alpha
SOD2	superoxide dismutase 2, mitochondrial
STAT3	signal transducer and activator of transcription 3 (acute-phase response factor)
VARS2	valyl-tRNA synthetase 2, mitochondrial