Human Phenotype Ontology 
Grandparent Node:
expandAbnormal atrial septum morphology (HP:0011994)help
Grandparent Node:
expandAbnormal cardiac atrium morphology (HP:0005120)help
Parent Node:
expandAtrial septal defect (HP:0001631)help
..Starting node
..expandSinus venosus atrial septal defect (HP:0011567)help
Term ID: 11567
Name: Sinus venosus atrial septal defect
Synonym:
Definition: An interatrial communication caused by a deficiency of the common wall between the superior vena cava (SVC) and the right-sided pulmonary veins. SVASD is commonly associated with anomalous pulmonary venous connection (APVC) of some or all of the pulmonary veins, which produces additional left-to-right shunting.
Comments:
Reference: HP:0011567
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandPatent foramen ovale (HP:0001655) help
..expandPrimum atrial septal defect (HP:0010445) help
..expandSecundum atrial septal defect (HP:0001684) help
..expandSwiss cheese atrial septal defect (HP:0031017) help
..expandUnroofed coronary sinus (HP:0031297) 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:0011567HP:0011567Sinus venosus atrial septal defect0 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.