Abnormality of the cardiac septa

Symptom Information:

Symptom ID: HPO:0001671
Synonyms:
Septal defects [HPO:0001671]
Atrial septal defect [Orphanet:34460]
Atrial septal defect (disorder) [Orphanet:34460]
Congenital atrial septal defect (disorder) [Orphanet:34460]
Interauricular septal defect (disorder) [Orphanet:34460]
Interauricular communication [Orphanet:34460]
Atrial Septal Defects [Orphanet:34460]
Septal defects [OMIM:Septal defects]
Atrial septal defect/interauricular communication [Orphanet:34460]
Atrial septal defect [MedDRA:10003664]
ASD [MedDRA:10003664]
Atrial septal defect NOS [MedDRA:10003664]
Congenital atrial septal defect [MedDRA:10003664]
Defect artrial septum [MedDRA:10003664]
Foramen ovale patent [MedDRA:10003664]
Heart septal defect atrial [MedDRA:10003664]
IA septal defect [MedDRA:10003664]
Interatrial foramen secundum defect [MedDRA:10003664]
Ostium primum defect [MedDRA:10003664]
Ostium secundum defect [MedDRA:10003664]
Ostium secundum type atrial septal defect [MedDRA:10003664]
Septal defect interatrial [MedDRA:10003664]
Septum atrial patent [MedDRA:10003664]
Interauricular communication [MedDRA:10003664]
Coronary sinus type atrial septal defect [MedDRA:10003664]
Atrial septal defect (1 patient) [OMIM:Atrial septal defect (1 patient)]
Atrial septal defect (1/4 patients) [OMIM:Atrial septal defect (1/4 patients)]
Atrial septal defect (2 patients) [OMIM:Atrial septal defect (2 patients)]
Atrial septal defect (ASD II) [OMIM:Atrial septal defect (ASD II)]
Atrial septal defect (in 1 patient) [OMIM:Atrial septal defect (in 1 patient)]
Atrial septal defect (in some patients) [OMIM:Atrial septal defect (in some patients)]
Atrial septal defect (less common) [OMIM:Atrial septal defect (less common)]
Atrial septal defect (male) [OMIM:Atrial septal defect (male)]
Atrial septal defect (ostium secundum type) [OMIM:Atrial septal defect (ostium secundum type)]
Atrial septal defect (rare) [OMIM:Atrial septal defect (rare)]
Atrial septal defect (uncommon) [OMIM:Atrial septal defect (uncommon)]
Atrial septal defects [OMIM:Atrial septal defects]
Patent foramen ovale (1 patient) [OMIM:Patent foramen ovale (1 patient)]
Patent foramen ovale (in one patient) [OMIM:Patent foramen ovale (in one patient)]
Patent foramen ovale (in some patients) [OMIM:Patent foramen ovale (in some patients)]
Quality:
Cross references:
HPO:0001631 "Defect in the atrial septum" [Orphanet:34460]
Orphanet:34460 "Atrial septal defect/interauricular communication" [Orphanet:34460]
OMIM: "Septal defects" [OMIM:Septal defects]
OMIM: "Atrial septal defect (1 patient)" [OMIM:Atrial septal defect (1 patient)]
OMIM: "Atrial septal defect (1/4 patients)" [OMIM:Atrial septal defect (1/4 patients)]
OMIM: "Atrial septal defect (2 patients)" [OMIM:Atrial septal defect (2 patients)]
OMIM: "Atrial septal defect (ASD II)" [OMIM:Atrial septal defect (ASD II)]
OMIM: "Atrial septal defect (in 1 patient)" [OMIM:Atrial septal defect (in 1 patient)]
OMIM: "Atrial septal defect (in some patients)" [OMIM:Atrial septal defect (in some patients)]
OMIM: "Atrial septal defect (less common)" [OMIM:Atrial septal defect (less common)]
OMIM: "Atrial septal defect (male)" [OMIM:Atrial septal defect (male)]
OMIM: "Atrial septal defect (ostium secundum type)" [OMIM:Atrial septal defect (ostium secundum type)]
OMIM: "Atrial septal defect (rare)" [OMIM:Atrial septal defect (rare)]
OMIM: "Atrial septal defect (uncommon)" [OMIM:Atrial septal defect (uncommon)]
OMIM: "Atrial septal defects" [OMIM:Atrial septal defects]
OMIM: "Patent foramen ovale (1 patient)" [OMIM:Patent foramen ovale (1 patient)]
OMIM: "Patent foramen ovale (in one patient)" [OMIM:Patent foramen ovale (in one patient)]
OMIM: "Patent foramen ovale (in some patients)" [OMIM:Patent foramen ovale (in some patients)]
UMLS:C2609256 "Interauricular communication" [Orphanet:34460]
UMLS:C0018817 "Atrial Septal Defects" [Orphanet:34460]
Is a (Direct Parents):
Orphanet Congenital septal defect
MedDRA Myocardial disorders NEC
HPO         obsolete Malformation of the heart and great vessels
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)
MedDRA:
Cardiac disorders(MedDRA:10007541)
    Abnormality of the myocardium(HPO:0001637)
       Myocardial disorders NEC(MedDRA:10028590)
          Abnormality of the cardiac septa(HPO:0001671)
Database Frequency: 55 / 7739
Resource:

All diseases associated with this symptom:

14q11.2 microdeletion syndrome (Orphanet:261120)
17q12 microduplication syndrome (Orphanet:261272)
ADAMS-OLIVER SYNDROME 4 (OMIM:615297)
APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIALDYSMORPHISM, AND OTHER CONGENITAL ANOMALIES (OMIM:300887)
ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 2 (OMIM:613404)
ATTRV122I amyloidosis (Orphanet:85451)
Acro-renal-ocular syndrome (Orphanet:959)
Acrocallosal syndrome (Orphanet:36)
Aldosterone-producing adenoma with seizures and neurological abnormalities (Orphanet:369929)
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency (Orphanet:331176)
BRACHYDACTYLY, TYPE E, WITH ATRIAL SEPTAL DEFECT, TYPE II (OMIM:113301)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CARPENTER SYNDROME 2 (OMIM:614976)
CHILD syndrome (Orphanet:139)
CHROMOSOME 15q25 DELETION SYNDROME (OMIM:614294)
Cardiomyopathy, familial hypertrophic, 13 (OMIM:613243)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Congenital heart block (Orphanet:60041)
Craniofacial dysplasia-osteopenia syndrome (Orphanet:314555)
Distal monosomy 10q (Orphanet:96148)
Distal monosomy 15q (Orphanet:1596)
Faisalabad histiocytosis (Orphanet:254707)
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (Orphanet:168566)
Floating-Harbor syndrome (Orphanet:2044)
H syndrome (Orphanet:168569)
HAJDU-CHENEY SYNDROME (OMIM:102500)
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 2 (OMIM:614749)
Hereditary orotic aciduria (Orphanet:30)
Holt-Oram syndrome (Orphanet:392)
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency (Orphanet:401948)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hypoplastic left heart syndrome (Orphanet:2248)
Intellectual deficit, X-linked - craniofacioskeletal syndrome (Orphanet:163979)
Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome (Orphanet:363611)
KABUKI SYNDROME 2 (OMIM:300867)
LOEYS-DIETZ SYNDROME 1 (OMIM:609192)
LOEYS-DIETZ SYNDROME 2 (OMIM:610168)
Lung agenesis - heart defect - thumb anomalies (Orphanet:1120)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Methylmalonic acidemia with homocystinuria, type cblJ (Orphanet:369955)
Mowat-Wilson syndrome (Orphanet:2152)
Myhre syndrome (Orphanet:2588)
NOONAN SYNDROME 1 (OMIM:163950)
Nephronophthisis 3 (OMIM:604387)
Okihiro syndrome (Orphanet:93293)
Pigmented hypertrichosis with insulin dependent diabetes mellitus syndrome (Orphanet:254723)
Rosaï-Dorfman disease (Orphanet:158014)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
Thiamine-responsive megaloblastic anemia syndrome (Orphanet:49827)
Thrombocytopenia - absent radius (Orphanet:3320)
VENTRICULAR SEPTAL DEFECT 1 (OMIM:614429)
VENTRICULAR SEPTAL DEFECT 3 (OMIM:614432)
VERHEIJ SYNDROME (OMIM:615583)
[DEL] ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1 (OMIM:208085)