Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Dilated cardiomyopathy due to phytanic acid storage disease |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Becker muscular dystrophy |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cardiac glycogen phosphorylase kinase deficiency |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Sturge-Weber syndrome |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Tophus of heart co-occurrent and due to gout |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Familial cardiomyopathy |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary oculoleptomeningeal amyloid angiopathy |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary cerebral amyloid angiopathy, Icelandic type |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary cerebral amyloid angiopathy, Dutch type |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Dilated cardiomyopathy due to glycogen storage disease |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Restrictive cardiomyopathy secondary to glycogen storage disease |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary coproporphyria |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Restrictive cardiomyopathy due to mucopolysaccharidosis |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Dilated cardiomyopathy due to mucopolysaccharidosis |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Jervell and Lange-Nielsen syndrome |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Pericarditis due to familial Mediterranean fever |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Jervell and Lange-Nielson syndrome |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary cutaneous vascular syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Ataxia-telangiectasia syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Familial hemiplegic migraine |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Danon disease |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Andersen Tawil syndrome |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Sturge-Weber syndrome |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Fatal congenital nonlysosomal heart glycogenosis |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary dysplasia of blood vessel |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Pulmonary hypertension in neurofibromatosis |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Heritable pulmonary arterial hypertension due to bone morphogenetic protein receptor type II mutation |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Blepharophimosis-intellectual disability syndrome Maat-Kievit-Brunner type |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Upshaw-Schulman syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Port-wine stain in Rubinstein-Taybi syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Dilated cardiomyopathy 3B |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Arrhythmogenic right ventricular dysplasia |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary cystatin C amyloid angiopathy |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Microcephaly-capillary malformation syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Capillary malformation-arteriovenous malformation syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
STING-associated vasculopathy with onset in infancy |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Glomuvenous malformation |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Transthyretin related familial amyloid cardiomyopathy |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Short stature with valvular heart disease and characteristic facies syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Potter sequence cleft lip and palate cardiopathy syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Isolated right ventricular hypoplasia |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Congenital heart defect with round face and developmental delay syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Moyamoya disease with early onset achalasia |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary arterial and articular multiple calcification syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Microcephalus with cardiac defect and lung malsegmentation syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Microcephalus cardiomyopathy syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Lethal faciocardiomelic dysplasia |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Vici syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Tubular renal disease with cardiomyopathy syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Timothy syndrome type 1 |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Timothy syndrome type 2 |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cardiac anomaly and heterotaxy syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cardiocranial syndrome Pfeiffer type |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cardiomyopathy with cataract and hip spine disease syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cardiomyopathy and renal anomaly syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cardiospondylocarpofacial syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Bosley Salih Alorainy syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Brachydactyly and arterial hypertension syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Braddock syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Arterial dissection and lentiginosis syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Aural atresia with multiple congenital anomalies and intellectual disability syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Cerebroretinal vasculopathy |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Ehlers-Danlos syndrome cardiac valvular type |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Ehlers-Danlos syndrome vascular-like type |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Holt-Oram syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Heart defect and limb shortening syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Heart-hand syndrome Slovenian type |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Short stature with webbed neck and congenital heart disease syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hydrocephalus, cardiac malformation, dense bone syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary vascular retinopathy |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Lung agenesis with heart defect and thumb anomaly syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Lymphedema, atrial septal defect, facial changes syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Lymphedema and cerebral arteriovenous anomaly syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Chronic atrial and intestinal dysrhythmia |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Isotretinoin embryopathy-like syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Kallman syndrome with heart disease |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Faciocardiorenal syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Fallot complex with intellectual disability and growth delay syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Polyvalvular heart disease syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Sensorineural deafness with dilated cardiomyopathy syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hereditary cerebral hemorrhage with amyloidosis |
Is a |
False |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Hepatic veno-occlusive disease with immunodeficiency syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|
Maternally inherited cardiomyopathy and hearing loss syndrome |
Is a |
True |
Cardiovascular system hereditary disorder |
Inferred relationship |
Existential restriction modifier |
|