Disorder of cardiovascular system	Hereditary disorder by system
\|	\|

Cardiovascular system hereditary disorder (disorder)
	Cardiovascular system hereditary disorder
	hereditaire aandoening van cardiovasculair systeem
	erfelijke aandoening van hart- en vaatstelsel erfelijke ziekte van tractus circulatorius

Id	363005004
Status	Defined

Finding site

Structure of cardiovascular system

ICD-10 complex map reference set

Target	I51.6
Rule	TRUE
Advice	ALWAYS I51.6
Correlation	SNOMED CT source code to target map code correlation not specified

Aneurysm osteoarthritis syndrome

Ankyrin-B syndrome

Aortic arch anomaly, facial dysmorphism, intellectual disability syndrome

Arrhythmogenic right ventricular dysplasia2

Arterial dissection and lentiginosis syndrome

Ataxia-telangiectasia syndrome

Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome

Atrial septal defect, atrioventricular conduction defect syndrome

Atrioventricular septal defect, blepharophimosis, radial and anal defect syndrome

Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome

Autosomal recessive sick sinus syndrome

Beemer Ertbruggen syndrome

Bosley Salih Alorainy syndrome

Brachydactyly and arterial hypertension syndrome

Braddock syndrome

Brugada syndrome

CAMOS syndrome

Capillary malformation-arteriovenous malformation syndrome

Cardiac anomaly and heterotaxy syndrome

Cardiac glycogen phosphorylase kinase deficiency

Cardiac glycogenosis

Cardiocranial syndrome Pfeiffer type

Cardiomyopathy and renal anomaly syndrome

Cardiomyopathy with cataract and hip spine disease syndrome

Cardiospondylocarpofacial syndrome

Carney complex

Cataract, congenital heart disease, neural tube defect syndrome

Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy

Chronic atrial and intestinal dysrhythmia

Cleft lip and cleft palate with intestinal malrotation and cardiopathy syndrome

Coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability ear anomaly syndrome

Combined oxidative phosphorylation defect type 17

Combined oxidative phosphorylation defect type 23

Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome

Congenital long QT syndrome7

Cooper Jabs syndrome

Danon disease

Dilated cardiomyopathy 3B

Dilated cardiomyopathy with hypergonadotropic hypogonadism syndrome

Disorder of cardiovascular system co-occurrent and due to Marfan syndrome1

Ehlers-Danlos syndrome cardiac valvular type

Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome

Erythrokeratodermia cardiomyopathy syndrome

Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome

Eye defects, arachnodactyly, cardiopathy syndrome

Fabry's disease

Facial dysmorphism, conductive hearing loss, heart defect syndrome

Facial dysmorphism, immunodeficiency, livedo, short stature syndrome

Faciocardiorenal syndrome

Fallot complex with intellectual disability and growth delay syndrome

Familial atrial tachyarrhythmia, infra-Hisian cardiac conduction disease

Familial bicuspid aortic valve1

Familial cerebral saccular aneurysm

Familial cervical artery dissection

Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome

Familial dilated cardiomyopathy with conduction defect due to LMNA mutation

Familial hemiplegic migraine

Familial patent arterial duct

Familial pulmonary capillary hemangiomatosis

Familial thoracic aortic aneurysm and aortic dissection

Fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease

Fatal congenital nonlysosomal heart glycogenosis

Fibrous skin tumor of tuberous sclerosis

Genitopalatocardiac syndrome

Glomuvenous malformation

Heart defect and limb shortening syndrome

Heart-hand syndrome Slovenian type

Hepatic veno-occlusive disease with immunodeficiency syndrome

Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome

Hereditary arterial and articular multiple calcification syndrome

Hereditary benign telangiectasia

Hereditary cavernous hemangioma of brain

Hereditary cerebrovascular amyloidosis1

Hereditary conduction disorder of the heart

Hereditary cutaneous vascular syndrome1

Hereditary diffuse endocapillary proliferative glomerulonephritis

Hereditary dysplasia of blood vessel4

Hereditary vascular fragility

Heritable pulmonary arterial hypertension due to BMPR2 mutation

Holt-Oram syndrome

Hypertension due to gain-of-function mutation in mineralocorticoid receptor

Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome

Hyperuricemia, pulmonary hypertension, renal failure, alkalosis syndrome

Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome

Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency

Intermediate epidermolysis bullosa simplex with cardiomyopathy

Isolated right ventricular hypoplasia

Isomerism of right atrial appendage

Isotretinoin-like syndrome

ITM2B-related amyloidosis2

Kallman syndrome with heart disease

Kartagener syndrome

Keutel syndrome

Larsen-like syndrome B3GAT3 type

Lethal arteriopathy syndrome due to fibulin-4 deficiency

Lethal brain and heart developmental defects syndrome

Lethal faciocardiomelic dysplasia

Lethal left ventricular non-compaction, seizures, hypotonia, cataract, developmental delay syndrome

Leukoencephalopathy with calcifications and cysts

Localized hereditary cardiac amyloidosis

Long QT syndrome type 10

Long QT syndrome type 11

Long QT syndrome type 12

Long QT syndrome type 13

Long QT syndrome type 2

Long QT syndrome type 3

Long QT syndrome type 4

Long QT syndrome type 5

Long thumb brachydactyly syndrome

Lung agenesis with heart defect and thumb anomaly syndrome

Lymphedema and cerebral arteriovenous anomaly syndrome

Lymphedema, atrial septal defect, facial changes syndrome

Macrocephaly, intellectual disability, left ventricular non compaction syndrome

Maternally inherited cardiomyopathy and hearing loss syndrome

Maternally inherited mitochondrial cardiomyopathy

Maternally inherited mitochondrial cardiomyopathy and myopathy

Megalencephaly capillary malformation

Microcephalus cardiomyopathy syndrome

Microcephalus with cardiac defect and lung malsegmentation syndrome

Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome

Microcephaly-capillary malformation syndrome

Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency

Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome

Moyamoya disease with early onset achalasia

Mucopolysaccharidosis-like plus disease

Multisystemic smooth muscle dysfunction syndrome

Muscle and heart glycogen synthase deficiency

Neonatal encephalomyopathy, cardiomyopathy, respiratory distress syndrome

Neonatal Marfan syndrome

Neonatal purpura fulminans (homozygous protein C deficiency)

Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome

Pancreatic hypoplasia, diabetes mellitus, congenital heart disease syndrome

Patent ductus arteriosus, bicuspid aortic valve, hand anomaly syndrome

Polyglucosan body myopathy type 1

Polysyndactyly and cardiac malformation syndrome

Polyvalvular heart disease syndrome

Pontine autosomal dominant microangiopathy with leukoencephalopathy

Port-wine stain in proteus syndrome

Port-wine stain in Rubinstein-Taybi syndrome

Postural orthostatic tachycardia syndrome due to norepinephrine transporter deficiency

Primary intraosseous venous malformation

Progressive sensorineural hearing loss and hypertrophic cardiomyopathy syndrome

Prune belly syndrome with pulmonic stenosis, mental retardation and deafness

Rambaud Gallian syndrome

Recurrent metabolic encephalomyopathic crises, rhabdomyolysis, cardiac arrhythmia, intellectual disability syndrome

Retinal arterial macroaneurysm with supravalvular pulmonic stenosis

Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations

Segmental outgrowth, lipomatosis, arteriovenous malformation, epidermal nevus syndrome

Sensorineural deafness with dilated cardiomyopathy syndrome

Severe hypotonia, psychomotor developmental delay, strabismus, cardiac septal defect syndrome

Short stature with valvular heart disease and characteristic facies syndrome

Short stature with webbed neck and congenital heart disease syndrome

Sinoatrial node dysfunction and deafness

Sonoda syndrome

STING-associated vasculopathy with onset in infancy

Subaortic stenosis and short stature syndrome

Thomas syndrome

TMEM94-associated congenital heart defect, facial dysmorphism, developmental delay syndrome

Transthyretin related familial amyloid cardiomyopathy

Tubular renal disease with cardiomyopathy syndrome

Upshaw-Schulman syndrome

Vasculitis due to adenosine deaminase 2 deficiency

Vici syndrome

White forelock with malformations syndrome

Wooly hair and palmoplantar keratoderma with dilated cardiomyopathy syndrome

X-linked intellectual disability, cardiomegaly, congestive heart failure syndrome