Patent foramen ovale

Symptom Information:

Symptom ID: HPO:0001655
Synonyms:
Patent foramen ovale [OMIM:Patent foramen ovale]
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:
OMIM: "Patent foramen ovale" [OMIM:Patent foramen ovale]
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)]
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 the cardiac septa(HPO:0001671)
                   Abnormality of the atrial septum(HPO:0011994)
                      Atria septal defect(HPO:0001631)
                         Patent foramen ovale(HPO:0001655)
                Abnormality of cardiac atrium(HPO:0005120)
                   Atria septal defect(HPO:0001631)
                      Patent foramen ovale(HPO:0001655)
MedDRA:
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

14q11.2 microdeletion syndrome (Orphanet:261120)
17p11.2 microduplication syndrome (Orphanet:1713)
1p36 deletion syndrome (Orphanet:1606)
ATRIAL SEPTAL DEFECT 4 (OMIM:611363)
Aldosterone-producing adenoma with seizures and neurological abnormalities (Orphanet:369929)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies (Orphanet:221145)
Dislocation of the hip - dysmorphism (Orphanet:2412)
Distal monosomy 6p (Orphanet:96125)
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 2 (OMIM:615539)
FIBROCHONDROGENESIS 1 (OMIM:228520)
Familial long QT syndrome (Orphanet:768)
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (Orphanet:168566)
Fibrochondrogenesis (Orphanet:2021)
HYPERTELORISM AND TETRALOGY OF FALLOT (OMIM:239711)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hypoplastic left heart syndrome 2 (OMIM:614435)
Larsen-like syndrome, B3GAT3 type (Orphanet:284139)
Microcephaly-capillary malformation syndrome (Orphanet:294016)
Mitochondrial DNA deletion syndrome with progressive myopathy (Orphanet:352470)
Neonatal hemochromatosis (Orphanet:446)
Nephronophthisis 9 (OMIM:613824)
Neu-Laxova syndrome (Orphanet:2671)
Pancreatic hypoplasia - diabetes - congenital heart disease (Orphanet:2255)
RIENHOFF SYNDROME (OMIM:615582)
RIGHT PULMONARY ARTERY, ANOMALOUS ORIGIN OF, FAMILIAL (OMIM:610338)
SKELETAL DYSPLASIA AND PROGRESSIVE CENTRAL NERVOUS SYSTEM DEGENERATION,LETHAL (OMIM:602613)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Timothy syndrome (Orphanet:65283)
Transaldolase deficiency (Orphanet:101028)
Transketolase deficiency (ORPHA:488618)