Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the cardiovascular system (HP:0001626)help
Parent Node:
expandAbnormal fetal cardiovascular morphology (HP:0010948)help
..Starting node
..expandPersistent fetal circulation (HP:0011726)help
Term ID: 11726
Name: Persistent fetal circulation
Synonym: Persistent foetal circulation
Definition: Systemic desaturation of a liveborn baby resulting from persistent pulmonary hypertension with a patent ductus arteriosus and patent foramen ovale, such that the circulation in postnatal life follows the fetal course.
Comments:
Reference: HP:0011726
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormality of ductus venosus blood flow (HP:0010947) help
..expandAbnormality of umbilical vein blood flow (HP:0010949) help
..expandCongenital portosystemic venous shunt (HP:0012022) help
..expandEchogenic intracardiac focus (HP:0010942) help
..expandPersistent patent ductus venosus (HP:0012021) help
..expandSingle umbilical artery (HP:0001195) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0011726HP:0011726Persistent fetal circulation0UQCRFS1 CL E G H738612587OMIM:618775MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 10; MC3DN10


Genes (1) :UQCRFS1

Diseases (1) :OMIM:618775
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.