Persistent Fetal Circulation Syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_13042)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D010547
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Genes

1 genes/proteins associated with the disease Persistent Fetal Circulation Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CPS1 carbamoyl-phosphate synthase 1, mitochondrial 2.88009