Human Phenotype Ontology 
Grandparent Node:
expandAbnormal pericardium morphology (HP:0001697)help
Parent Node:
expandPericardial effusion (HP:0001698)help
..Starting node
..expandChylopericardium (HP:0011852)help
Term ID: 11852
Name: Chylopericardium
Synonym:
Definition: Accumulation of chyle (the whitish fluid taken up by the lacteals in the intestine, consisting of an emulsion of lymph and triglyceride fat thatpasses into the veins by the thoracic duct) in the pericardium. Chylopericardium is generally caused by obstruction of or trauma to the thoracic duct.
Comments:
Reference: HP:0011852
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandHemopericardium (HP:0011851) help
..expandSerous pericardial effusion (HP:0011853) 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:0011852HP:0011852Chylopericardium0TSC1 CL E G H724812362ORPHA:538LymphangioleiomyomatosisHP:0040283 - Occasional1090
HP:0011852HP:0011852Chylopericardium0TSC2 CL E G H724912363ORPHA:538LymphangioleiomyomatosisHP:0040283 - Occasional2738


Genes (2) :TSC1 TSC2

Diseases (1) :ORPHA:538
 

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