Human Phenotype Ontology 
Grandparent Node:
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Abnormal myocardium morphology (HP:0001637)help
Parent Node:
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Cardiomyopathy (HP:0001638)help
..Starting node
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Takotsubo cardiomyopathy (HP:0011665)help
Term ID: 11665
Name: Takotsubo cardiomyopathy
Synonym: Broken-heart syndrome
Definition: Transient left ventricular apical ballooning syndrome or takotsubo cardiomyopathy is characterized by transient regional systolic dysfunction involving the left ventricular apex and/or mid-ventricle in the absence of obstructive coronary disease on coronary angiography. Patients present with an abrupt onset of angina-like chest pain, and have diffuse T-wave inversion, sometimes preceded by ST-segment elevation, and mild cardiac enzyme elevation.
Comments:
Reference: HP:0011665
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAtrial cardiomyopathy (HP:0200127) help
..expandDilated cardiomyopathy (HP:0001644) help
..expandHistiocytoid cardiomyopathy (HP:0005152) help
..expandHypertrophic cardiomyopathy (HP:0001639) help
..expandNoncompaction cardiomyopathy (HP:0012817) help
..expandRestrictive cardiomyopathy (HP:0001723) help
..expandRight ventricular cardiomyopathy (HP:0011663) 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:0011665HP:0011665Takotsubo cardiomyopathy0ADORA2A CL E G H135263ORPHA:363549Acute encephalopathy with biphasic seizures and late reduced diffusionHP:0040284 - Very rare1


Genes (1) :ADORA2A

Diseases (1) :ORPHA:363549
 

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