Human Phenotype Ontology 
Grandparent Node:
expandAbnormal myocardium morphology (HP:0001637)help
Parent Node:
expandCardiomyopathy (HP:0001638)help
..Starting node
..expandAtrial cardiomyopathy (HP:0200127)help
Term ID: 200127
Name: Atrial cardiomyopathy
Synonym:
Definition: Any complex of structural, architectural, contractile or electrophysiological changes affecting the atria with the potential to produce clinically relevant manifestations.
Comments:
Reference: HP:0200127
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..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
..expandTakotsubo cardiomyopathy (HP:0011665) 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:0200127HP:0200127Atrial cardiomyopathy0GJA5 CL E G H27024279OMIM:108770Atrial standstill 1.39
HP:0200127HP:0200127Atrial cardiomyopathy0NPPA CL E G H48787939OMIM:615745Atrial standstill 213


Genes (2) :GJA5 NPPA

Diseases (2) :OMIM:108770 OMIM:615745
 

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