Human Phenotype Ontology 
Grandparent Node:
expandPhenotypic abnormality (HP:0000118)help
Parent Node:
expandAbnormality of the cardiovascular system (HP:0001626)help
..Starting node
..expandAbnormality of the fetal cardiovascular system (HP:0010948)help
Term ID: 10948
Name: Abnormality of the fetal cardiovascular system
Synonym: Abnormality of the fetal circulation system; Abnormality of the foetal cardiovascular system; Abnormality of the foetal circulation system
Definition: An abnormality of the fetal circulation system or fetal echocardiogram.
Comments:
Reference: HP:0010948
Genes and Diseases:
 
       Child Nodes:
........expandSingle umbilical artery (HP:0001195) help
........expandEchogenic intracardiac focus (HP:0010942) help
........expandAbnormality of ductus venosus blood flow (HP:0010947) help
........expandAbnormality of umbilical vein blood flow (HP:0010949) help
........expandPersistent fetal circulation (HP:0011726) help
........expandPersistent patent ductus venosus (HP:0012021) help
........expandCongenital portosystemic venous shunt (HP:0012022) help

 Sister Nodes: 
..expandAbnormal cardiovascular system physiology (HP:0011025) help
..expandAbnormality of cardiovascular system morphology (HP:0030680) help
..expandAbnormality of the vasculature (HP:0002597) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010948HP:0010948Abnormality of the fetal cardiovascular system0 CL E G H
HP:0010948HP:0010947Abnormality of ductus venosus blood flow1 CL E G H
HP:0010948HP:0010942Echogenic intracardiac focus1 CL E G H
HP:0010948HP:0012021Persistent patent ductus venosus1 CL E G H
HP:0010948HP:0001195Single umbilical artery1 CL E G H
HP:0010948HP:0011726Persistent fetal circulation1 CL E G H
HP:0010948HP:0010949Abnormality of umbilical vein blood flow1 CL E G H
HP:0010948HP:0012022Congenital portosystemic venous shunt1 CL E G H


Genes (12) :CCDC22 FANCB FOXF1 GATA6 HOXD13 MCTP2 MKS1 PACS1 SCARF2 TAPT1 WASHC5 WNT3

Diseases (13) :7 3412 210122 2255 600001 887 1596 249000 615009 600920 616897 220210 273395
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.