Secundum atrial septal defect
Symptom Information:
Symptom ID: | HPO:0001684 | ||
Synonyms: |
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Is a (Direct Parents): |
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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 the cardiac septa(HPO:0001671) Abnormality of the atrial septum(HPO:0011994) Atria septal defect(HPO:0001631) Secundum atrial septal defect(HPO:0001684) Abnormality of cardiac atrium(HPO:0005120) Atria septal defect(HPO:0001631) Secundum atrial septal defect(HPO:0001684) MedDRA: |
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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) |