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762228008: Congenital cardiovascular disorder (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3636221017 Congenital cardiovascular disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3636222012 Congenital cardiovascular disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3636221017 Congenital cardiovascular disorder (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3636222012 Congenital cardiovascular disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5856361000241113 affection cardiovasculaire congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5856361000241113 affection cardiovasculaire congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


1630 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital cardiovascular disorder (disorder) Is a Disorder of cardiovascular system true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cardiovascular disorder (disorder) Is a Congenital disease true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cardiovascular disorder (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital cardiovascular disorder (disorder) Finding site Structure of cardiovascular system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital anomaly of cardiovascular system Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Rubella myocarditis (disorder) Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital stenosis of cardiac valve Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cardiac failure (disorder) Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital His bundle tachycardia Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital peripheral aneurysm Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital conduction defect Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital vascular disorder Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Fenestrated interatrial communication within oval fossa (disorder) Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital stenosis of mitral subvalvular apparatus Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital pericardial effusion (disorder) Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder) Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder) Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
This syndrome is characterized by the association of dilated cardiomyopathy and hypergonadotropic hypogonadism (DCM-HH). Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cardiomyopathy and renal anomaly syndrome (disorder) Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Heart-hand syndrome Slovenian type (disorder) Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Hydrocephalus with endocardial fibroelastosis and cataract syndrome (disorder) Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Glycogen storage disease due to muscle and heart glycogen synthase deficiency is characterized by muscle and heart glycogen deficiency. It has been described in three siblings (two brothers and their younger sister). The older brother died at 10.5 years of age as a result of sudden cardiac arrest and the younger brother presented with hypertrophic cardiomyopathy, abnormal heart rate and blood pressure during exercise, and muscle fatigability. The sister showed no symptoms but a lack of glycogen was identified through muscle biopsy. The syndrome is caused by homozygous missense mutations in the gene encoding muscle glycogen synthase. Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Long thumb brachydactyly syndrome (disorder) Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Carney complex (disorder) Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of atrioventricular valve Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital anomaly of atrioventricular septum Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Ankyrin-B syndrome Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Carney complex, trismus, pseudocamptodactyly syndrome (disorder) Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital septal defect of heart Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Sinoatrial node dysfunction and deafness (disorder) Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Patent foramen ovale Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cyanotic congenital heart disease Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Tripartite right ventricle Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Posterior deviation of infundibular septum of obstructive aortic arch type (disorder) Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome (disorder) Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Timothy syndrome type 1 Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Timothy syndrome type 2 (disorder) Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Familial long QT syndrome Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital dysplasia of truncal valve Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital hypoplasia of anulus fibrosus of aorta Is a False Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Late congenital cardiovascular syphilis Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Endocardial fibroelastosis of right atrium Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Endocardial fibroelastosis of left atrium (disorder) Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Cardiac glycogenosis (disorder) Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Congenital rhabdomyoma of heart Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Eye defects, arachnodactyly, cardiopathy syndrome Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Timothy syndrome Is a True Congenital cardiovascular disorder (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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