Perimembranous ventricular septal defect
Symptom Information:
Symptom ID: | HPO:0011682 | ||||||||
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 ventricular septum(HPO:0010438) Ventricular septal defect(HPO:0001629) Perimembranous ventricular septal defect(HPO:0011682) Abnormality of cardiac ventricle(HPO:0001713) Abnormality of the ventricular septum(HPO:0010438) Ventricular septal defect(HPO:0001629) Perimembranous ventricular septal defect(HPO:0011682) MedDRA: |
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Database Frequency: | 6 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
Alpha-thalassemia - X-linked intellectual deficit syndrome | (Orphanet:847) |
CARDIAC SEPTAL DEFECTS WITH COARCTATION OF THE AORTA | (OMIM:212090) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
MUNGAN SYNDROME | (OMIM:611376) |
Pancreatic hypoplasia - diabetes - congenital heart disease | (Orphanet:2255) |
VENTRICULAR SEPTAL DEFECT 2 | (OMIM:614431) |