Secundum atrial septal defect

Symptom Information:

Symptom ID: HPO:0001684
Synonyms:
Secundum atrial septal defect [OMIM:Secundum atrial septal defect]
Atrial septal defect, secundum type [OMIM,du]
Quality:
Cross references:
OMIM: "Secundum atrial septal defect" [OMIM:Secundum atrial septal defect]
Is a (Direct Parents):
HPO         Atria septal defect
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormal heart morphology(HPO:0001627)
             obsolete Malformation of the heart and great vessels(HPO:0002564)
                Abnormality of cardiac atrium(HPO:0005120)
                   Atria septal defect(HPO:0001631)
                      Secundum atrial septal defect(HPO:0001684)
                Abnormality of the cardiac septa(HPO:0001671)
                   Abnormality of the atrial septum(HPO:0011994)
                      Atria septal defect(HPO:0001631)
                         Secundum atrial septal defect(HPO:0001684)
MedDRA:
Database Frequency: 14 / 7739
Resource:

All diseases associated with this symptom:

AICA-ribosiduria (Orphanet:250977)
ATRIAL SEPTAL DEFECT 3 (OMIM:614089)
ATRIAL SEPTAL DEFECT 9 (OMIM:614475)
Atrial septal defect - atrioventricular conduction defects syndrome (Orphanet:1479)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
CARDIAC SEPTAL DEFECTS WITH COARCTATION OF THE AORTA (OMIM:212090)
Cardiomyopathy, dilated, 1AA with or without left ventricular noncompaction (OMIM:612158)
His bundle tachycardia (Orphanet:3283)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Lung fibrosis - immunodeficiency - 46,XX gonadal dysgenesis (Orphanet:137631)
Microgastria - limb reduction defect (Orphanet:2538)
Neonatal hemochromatosis (Orphanet:446)
PULMONIC STENOSIS, ATRIAL SEPTAL DEFECT, AND UNIQUE ELECTROCARDIOGRAPHICABNORMALITIES (OMIM:178650)
[DEL] NEUROFIBROMATOSIS-NOONAN SYNDROME (OMIM:601321)