Human Phenotype Ontology 
Grandparent Node:
expandAbnormal heart morphology (HP:0001627)help
Parent Node:
expandAbnormal cardiac atrium morphology (HP:0005120)help
..Starting node
..expandCor triatriatum (HP:0010774)help
Term ID: 10774
Name: Cor triatriatum
Synonym: Triatrial heart
Definition: The presence of an additional membrane in the left or right cardiac atrium which results in the subdivision of the affected atrium (and thus in total three atria, whence the name).
Comments:
Reference: HP:0010774
Genes and Diseases:
 
       Child Nodes:
........expandCor triatriatum dexter (HP:0011566) help
........expandCor triatrium sinister (HP:0031134) help

 Sister Nodes: 
..expandAbnormal atrial arrangement (HP:0011535) help
..expandAbnormal coronary sinus morphology (HP:0011642) help
..expandAbnormal left atrium morphology (HP:0025579) help
..expandAbnormal right atrium morphology (HP:0025580) help
..expandAtrial septal defect (HP:0001631) help
..expandAtrial septal hypertrophy (HP:0031296) help
..expandCommon atrium (HP:0011565) 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:0010774HP:0010774Cor triatriatum0G6PC3 CL E G H9257924861OMIM:612541Neutropenia, severe congenital, 4, autosomal recessive.37
HP:0010774HP:0010774Cor triatriatum0MYRF CL E G H7451181OMIM:618280Cardiac-Urogenital syndrome2
HP:0010774HP:0010774Cor triatriatum0TTC26 CL E G H7998921882OMIM:619534BILIARY, RENAL, NEUROLOGIC, AND SKELETAL SYNDROME; BRENS
HP:0010774HP:0011566Cor triatriatum dexter1 CL E G H
HP:0010774HP:0031134Cor triatrium sinister1MYRF CL E G H7451181OMIM:618280Cardiac-Urogenital syndrome2


Genes (3) :G6PC3 MYRF TTC26

Diseases (3) :OMIM:612541 OMIM:618280 OMIM:619534
 

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