Human Phenotype Ontology 
Grandparent Node:
expandAbnormal heart morphology (HP:0001627)help
Parent Node:
expandAbnormal myocardium morphology (HP:0001637)help
..Starting node
..expandFocal necrosis of right ventricular muscle cells (HP:0003338)help
Term ID: 3338
Name: Focal necrosis of right ventricular muscle cells
Synonym:
Definition:
Comments:
Reference: HP:0003338
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal morphology of myocardial trabeculae (HP:0030681) help
..expandAbnormal ventricular myocardium morphology (HP:0031316) help
..expandCardiac amyloidosis (HP:0030843) help
..expandCardiomyopathy (HP:0001638) help
..expandFatty replacement of ventricular myocardial tissue (HP:0031317) help
..expandMyocardial fibrosis (HP:0001685) help
..expandMyocardial immune cell infiltration (HP:0031321) help
..expandMyocardial necrosis (HP:0001700) help
..expandMyocarditis (HP:0012819) help
..expandMyofiber disarray (HP:0031318) 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:0003338HP:0003338Focal necrosis of right ventricular muscle cells0 CL E G H


Genes (0) :

Diseases (0) :
 

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