Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Heritable pulmonary arterial hypertension due to BMPR2 mutation |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Ohdo syndrome, Maat-Kievit-Brunner type |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Upshaw-Schulman syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Port-wine stain in Rubinstein-Taybi syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Dilated cardiomyopathy 3B (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome autosomique dominant d'hématurie, tortuosités rétiniennes, crampes musculaires |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Arrhythmogenic right ventricular dysplasia (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Hereditary cystatin C amyloid angiopathy (disorder) |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Microcephaly-capillary malformation syndrome |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Capillary malformation-arteriovenous malformation syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Dilated cardiomyopathy due to phytanic acid storage disease |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Becker muscular dystrophy |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
STING-associated vasculopathy with onset in infancy (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
malformation glomuveineuse |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Transthyretin related familial amyloid cardiomyopathy (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Short stature with valvular heart disease and characteristic facies syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Potter sequence cleft lip and palate cardiopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Isolated right ventricular hypoplasia (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Sonoda syndrome |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Moyamoya disease with early onset achalasia (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome héréditaire de calcification artérielle et articulaire |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Microcephalus with cardiac defect and lung malsegmentation syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Microcephalus cardiomyopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Lethal faciocardiomelic dysplasia (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Vici syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Naxos disease |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Woolly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Tubular renal disease with cardiomyopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Timothy syndrome type 1 (disorder) |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Timothy syndrome type 2 (disorder) |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Cardiac anomaly and heterotaxy syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Cardiocranial syndrome Pfeiffer type (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Cardiomyopathy with cataract and hip spine disease syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Cardiomyopathy and renal anomaly syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Cardiospondylocarpofacial syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome d'athérosclérose, surdité, épilepsie, diabète, néphropathie |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Bosley Salih Alorainy syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Brachydactyly and arterial hypertension syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Braddock syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Arterial dissection and lentiginosis syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Aural atresia with multiple congenital anomalies and intellectual disability syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Cerebroretinal vasculopathy (disorder) |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Ehlers-Danlos syndrome cardiac valvular type (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Ehlers-Danlos syndrome vascular-like type (disorder) |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome de Holt-Oram |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Heart defect and limb shortening syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Heart-hand syndrome Slovenian type (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Short stature with webbed neck and congenital heart disease syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome léthal d'hydrocéphalie, malformation cardiaque, hyperdensité osseuse |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Hereditary vascular retinopathy (disorder) |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome (disorder) |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Lung agenesis with heart defect and thumb anomaly syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Lymphedema, atrial septal defect, facial changes syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Lymphedema and cerebral arteriovenous anomaly syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Chronic atrial and intestinal dysrhythmia (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Isotretinoin embryopathy-like syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Kallman syndrome with heart disease (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Faciocardiorenal syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome de tétralogie de Fallot-petite taille-déficience intellectuelle |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome d'hypotrichose, lymphœdème, télangiectasie, atteinte rénale |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome de la maladie cardiaque polyvalvulaire |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Sensorineural deafness with dilated cardiomyopathy syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Hereditary cerebral hemorrhage with amyloidosis (disorder) |
est un(e) (attribut) |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Hepatic veno-occlusive disease with immunodeficiency syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Maternally inherited cardiomyopathy and hearing loss syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Keutel syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Muscle and heart glycogen synthase deficiency (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Polysyndactyly and cardiac malformation syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Atrial septal defect, atrioventricular conduction defect syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome d'ataxie cérébelleuse, déficience intellectuelle, atrophie optique, anomalies cutanées |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Cataract, congenital heart disease, neural tube defect syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Carney complex (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Long thumb brachydactyly syndrome |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Disorder of cardiovascular system co-occurrent and due to Marfan syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome de cardiopathie, blépharophimosis, anomalie du radius, anomalie anale |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome de dysmorphie faciale, surdité de transmission, malformation cardiaque |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome de mèches blanches et anomalies multiples |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome de Larsen-like de type B3GAT3 (beta-1,3 glucuronyltransferase 3) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
syndrome de Marfan néonatal |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Primary intraosseous venous malformation (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Retinal arterial macroaneurysm with supravalvular pulmonic stenosis |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Ankyrin-B syndrome |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Familial thoracic aortic aneurysm and aortic dissection |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Familial dilated cardiomyopathy with conduction defect due to LMNA mutation |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|
Familial bicuspid aortic valve (disorder) |
est un(e) (attribut) |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Some |
|