Perimembranous ventricular septal defect

Symptom Information:

Symptom ID: HPO:0011682
Synonyms:
Conoventricular ventricular septal defect [HPO:0011682]
Membranous ventricular septal defect [HPO:0011682]
Paramembranous ventricular septal defect [HPO:0011682]
Type 2 ventricular septal defect [HPO:0011682]
VENTRICULAR SEPTAL DEFECT, PERIMEMBRANOUS [HPO:0011682]
Perimembranous ventricular septal defect [OMIM:Perimembranous ventricular septal defect]
Ventricular septal defect, perimembranous [OMIM:Ventricular septal defect, perimembranous]
Ventricular septal defect, membranous [OMIM:Ventricular septal defect, membranous]
Quality:
Cross references:
OMIM: "Perimembranous ventricular septal defect" [OMIM:Perimembranous ventricular septal defect]
OMIM: "Ventricular septal defect, perimembranous" [OMIM:Ventricular septal defect, perimembranous]
OMIM: "Ventricular septal defect, membranous" [OMIM:Ventricular septal defect, membranous]
Is a (Direct Parents):
HPO         Ventricular 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 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:
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)