Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Ventricular septal defect |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Common ventricle |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Atrial septal defect |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital atrial septal defect (disorder) |
Is a |
True |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Atrioventricular septal defect and common atrioventricular junction |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ebstein's anomaly with atrial septal defect |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Lymphedema-atrial septal defects-facial changes syndrome is characterized by congenital lymphedema of the lower limbs, atrial septal defect and a characteristic facies (a round face with a prominent forehead, a flat nasal bridge with a broad nasal tip, epicanthal folds, a thin upper lip and a cleft chin). It has been described in two brothers and a sister. Transmission appears to be autosomal recessive. |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Acquired abnormality of atrioventricular (not morphologically mitral or tricuspid) valve associated with atrioventricular septal defect |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fenestrated interatrial communication within oval fossa (disorder) |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Endocardial cushion defect |
Is a |
True |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital ventricular septal defect |
Is a |
True |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Eisenmenger's syndrome (disorder) |
Is a |
True |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Atrioventricular septal defect with atrioventricular valve regurgitation (disorder) |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Cor triloculare |
Is a |
True |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Double outlet right ventricle with subaortic ventricular septal defect and pulmonary stenosis Fallot type (disorder) |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transposition of great arteries with concordant atrioventricular connections and ventricular septal defect (disorder) |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transposition of great arteries with concordant atrioventricular connections and ventricular septal defect and left ventricular outflow tract obstruction (disorder) |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Atrioventricular septal defect with ventricular imbalance |
Is a |
False |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome is a rare, genetic, non-dystrophic congenital myopathy disorder characterized by a neonatal-onset of severe generalized hypotonia associated with mild psychomotor delay, congenital strabismus with abducens nerve palsy, and atrial and/or ventricular septal defects. Cryptorchidism is commonly reported in male patients and muscle biopsy typically reveals increased variability in muscle fiber size. |
Is a |
True |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital atrioventricular septal defect (disorder) |
Is a |
True |
Congenital septal defect of heart |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|