Name: Cardiovascular system hereditary disorder (disorder)
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- Cardiovascular system hereditary disorder
- Cardiovascular system hereditary disorder (disorder)
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Concept ID: 363005004- Cardiovascular system hereditary disorder (disorder)
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ICD-10 Codes: I516
- Andersen Tawil syndrome (disorder)
- Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome
- + Arrhythmogenic right ventricular dysplasia (disorder)
- Arterial dissection and lentiginosis syndrome
- Ataxia-telangiectasia syndrome
- Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome
- Atrial septal defect, atrioventricular conduction defect syndrome (disorder)
- Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome (disorder)
- Bosley Salih Alorainy syndrome (disorder)
- Brachydactyly and arterial hypertension syndrome (disorder)
- Braddock syndrome (disorder)
- CAMOS syndrome
- Capillary malformation-arteriovenous malformation syndrome
- Cardiac anomaly and heterotaxy syndrome
- Cardiac arrhythmia ankyrin-B related (disorder)
- Cardiac glycogen phosphorylase kinase deficiency (disorder)
- Cardiocranial syndrome Pfeiffer type (disorder)
- Cardiomyopathy and renal anomaly syndrome (disorder)
- Cardiomyopathy with cataract and hip spine disease syndrome (disorder)
- Cardiospondylocarpofacial syndrome
- Carney complex (disorder)
- Cataract, congenital heart disease, neural tube defect syndrome (disorder)
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Cerebroretinal vasculopathy
- Chronic atrial and intestinal dysrhythmia
- Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome (disorder)
- Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome (disorder)
- Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
- Cooper Jabs syndrome
- Danon disease (disorder)
- Dilated cardiomyopathy 3B
- Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome (disorder)
- + Disorder of cardiovascular system co-occurrent and due to Marfan syndrome
- Ehlers-Danlos syndrome cardiac valvular type
- Ehlers-Danlos syndrome vascular-like type
- Facial dysmorphism, conductive hearing loss, heart defect syndrome (disorder)
- Faciocardiorenal syndrome (disorder)
- Fallot complex with intellectual disability and growth delay syndrome (disorder)
- Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation (disorder)
- Familial hemiplegic migraine (disorder)
- Familial thoracic aortic aneurysm and aortic dissection
- Fatal congenital nonlysosomal heart glycogenosis (disorder)
- Glomuvenous malformation (disorder)
- HANAC - hereditary angiopathy with nephropathy, aneurysms, and muscle cramps
- Heart defect and limb shortening syndrome (disorder)
- Heart-hand syndrome Slovenian type (disorder)
- Hepatic veno-occlusive disease with immunodeficiency syndrome
- Hereditary arterial and articular multiple calcification syndrome
- + Hereditary cerebral haemorrhage with amyloidosis
- + Hereditary cutaneous vascular syndrome
- Hereditary cystatin C amyloid angiopathy
- + Hereditary dysplasia of blood vessel (disorder)
- Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome
- Hereditary oculoleptomeningeal amyloid angiopathy (disorder)
- Hereditary vascular retinopathy (disorder)
- Heritable pulmonary arterial hypertension due to BMPR2 mutation
- Holt-Oram syndrome
- Hydrocephalus, cardiac malformation, dense bone syndrome (disorder)
- Hypertension due to gain-of-function mutation in mineralocorticoid receptor (disorder)
- Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder)
- Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome (disorder)
- Isolated right ventricular hypoplasia
- Isotretinoin-like syndrome
- Jervell and Lange-Nielsen syndrome
- Kallman syndrome with heart disease
- Keratosis palmoplantaris and arrhythmogenic cardiomyopathy syndrome (disorder)
- Keutel syndrome
- Larsen-like syndrome beta-1,3-glucuronyltransferase 3 type (disorder)
- Lethal faciocardiomelic dysplasia (disorder)
- Long thumb brachydactyly syndrome (disorder)
- Lung agenesis with heart defect and thumb anomaly syndrome (disorder)
- Lymphoedema and cerebral arteriovenous anomaly syndrome
- Lymphoedema, atrial septal defect, facial changes syndrome
- Maternally inherited cardiomyopathy and hearing loss syndrome
- Microcephalus cardiomyopathy syndrome
- Microcephalus with cardiac defect and lung malsegmentation syndrome
- Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome (disorder)
- Microcephaly-capillary malformation syndrome
- Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation (disorder)
- Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome
- Moyamoya disease with early onset achalasia (disorder)
- Muscle and heart glycogen synthase deficiency
- Neonatal Marfan syndrome
- Ohdo syndrome, Maat-Kievit-Brunner type
- Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome
- Patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome (disorder)
- Pericarditis associated with familial Mediterranean fever
- Polysyndactyly and cardiac malformation syndrome
- Polyvalvular heart disease syndrome
- Port-wine stain in Rubinstein-Taybi syndrome
- Potter sequence cleft lip and palate cardiopathy syndrome (disorder)
- Primary intraosseous venous malformation
- Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome (disorder)
- Pulmonary hypertension in neurofibromatosis
- Retinal arterial macroaneurysm with supravalvular pulmonic stenosis
- Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder)
- Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal naevus syndrome
- Sensorineural deafness with dilated cardiomyopathy syndrome (disorder)
- Short stature with valvular heart disease and characteristic facies syndrome
- Short stature with webbed neck and congenital heart disease syndrome
- Sonoda syndrome
- STING-associated vasculopathy with onset in infancy (disorder)
- Timothy syndrome type 1 (disorder)
- Timothy syndrome type 2 (disorder)
- Transthyretin related familial amyloid cardiomyopathy (disorder)
- Tubular renal disease with cardiomyopathy syndrome
- Upshaw-Schulman syndrome
- Vici syndrome
- White forelock with malformations syndrome
- Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome (disorder)