FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.22-SNAPSHOT  |  FHIR Version n/a  User: [n/a]

24964005: Cardiac conducting system structure (body structure)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
41844011 Cardiac conduction system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
482071012 Cardiac conducting system structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
754660010 Cardiac conducting system structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
12411000077113 structure du système de conduction cardiaque fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

85 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cardiac conducting system structure Is a Cardiac internal structure true Inferred relationship Some
Cardiac conducting system structure partie de Entire heart false Additional relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
A broad spectrum of other macroreentrant tachycardias in which the wave front does not travel around the tricuspid annulus. Atypical atrial flutter originates from the left atrium or areas in the right atrium (such as surgical scars) and has a variable appearance on ECG in regards to the flutter waves. Finding site True Cardiac conducting system structure Inferred relationship Some 2
A rare autosomal dominant heart-hand syndrome that is characterized by bisymmetric brachydactyly accompanied by long thumbs, joint anomalies (restriction of motion at the shoulder and metacarpophalangeal joints) and cardiac conduction defects. Additional features include small hands and feet, clinodactyly, narrow shoulders with short clavicles, pectus excavatum and mild shortness of the limbs, cardiomegaly and murmur of pulmonic stenosis. There have been no new reports since 1981. Finding site True Cardiac conducting system structure Inferred relationship Some 5
Cardiac arrest due to administration of anesthesia in pregnancy Finding site True Cardiac conducting system structure Inferred relationship Some 3
A rare group of genetic, cardiac rhythm diseases with characteristics of a prolongation of the QT interval at basal electrocardiography (ECG) and by a high risk of life-threatening arrhythmias. The two cardinal manifestations are syncopal episodes, which may lead to cardiac arrest and sudden cardiac death, and electrocardiographic abnormalities: prolongation of the QT interval and T wave abnormalities. Inheritance may be autosomal dominant or autosomal recessive and depends on the genes involved. Finding site True Cardiac conducting system structure Inferred relationship Some 1
Cardiac arrest due to failed attempted abortion Finding site True Cardiac conducting system structure Inferred relationship Some 2
Cardiac arrest due to miscarriage Finding site True Cardiac conducting system structure Inferred relationship Some 2
Cardiac arrest due to incomplete miscarriage (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 2
Induced termination of pregnancy complicated by cardiac arrest Finding site True Cardiac conducting system structure Inferred relationship Some 1
Cardiac arrest following obstetric procedure (disorder) Finding site False Cardiac conducting system structure Inferred relationship Some 3
Recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome is a rare, genetic, neurodegenerative disease characterized by episodic metabolic encephalomyopathic crises (of variable frequency and severity which are frequently precipitated by an acute illness) which manifest with profound muscle weakness, ataxia, seizures, cardiac arrhythmias, rhabdomyolysis with myoglobinuria, elevated plasma creatine kinase, hypoglycemia, lactic acidosis, increased acylcarnitines and a disorientated or comatose state. Global developmental delay, intellectual disability and cortical, pyramidal and cerebellar signs develop with subsequent progressive neurodegeneration causing loss of expressive language and varying degrees of cerebral atrophy. Finding site True Cardiac conducting system structure Inferred relationship Some 4
A rare genetic disease characterized by intellectual disability, developmental delay, language deficits, and cardiac arrhythmia (most commonly sick sinus syndrome). Additional reported features include epilepsy, hypotonia, retinal abnormalities, nystagmus, attention deficit hyperactivity disorder, autism, and gastroesophageal reflux. The severity of the phenotype is highly variable. Finding site True Cardiac conducting system structure Inferred relationship Some 1
A rare subtype of autosomal recessive limb-girdle muscular dystrophy characterized by atrioventricular block resulting in repeated syncope episodes, elevated creatine kinase serum levels and adult-onset of slowly progressive proximal limb skeletal muscle weakness and atrophy. Muscular dystrophic changes observed in muscle biopsy include diameter variability, increased central nuclei, and presence of necrotic and regenerating fibers. Finding site True Cardiac conducting system structure Inferred relationship Some 3
Cardiac arrest during surgery (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 2
Arrhythmia during surgery (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Intraoperative cardiorespiratory arrest (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 2
Postoperative cardiopulmonary failure Finding site True Cardiac conducting system structure Inferred relationship Some 2
Cardiac arrest AND/OR failure following anesthesia AND/OR sedation in labor AND/OR delivery Finding site True Cardiac conducting system structure Inferred relationship Some 5
Cardiac arrhythmia due to coronary artery spasm Finding site True Cardiac conducting system structure Inferred relationship Some 1
Long QT syndrome type 9 Finding site True Cardiac conducting system structure Inferred relationship Some 1
Long QT syndrome type 6 (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Long QT syndrome type 4 (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Long QT syndrome type 5 (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Long QT syndrome type 2 (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Long QT syndrome type 11 (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Long QT syndrome type 10 (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Long QT syndrome type 3 (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Long QT syndrome type 12 (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Long QT syndrome type 13 (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Neonatal cardiorespiratory arrest Finding site True Cardiac conducting system structure Inferred relationship Some 3
Arrhythmia due to vegetation of infective endocarditis Finding site True Cardiac conducting system structure Inferred relationship Some 2
Cardiac arrest due to procedure (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Cardiac arrest during procedure (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
A rare multiple congenital anomalies syndrome with cardiac involvement as a major feature with characteristics of QT prolongation, congenital heart defects, syndactyly, facial dysmorphism and neurodevelopmental features. The atypical form (ATS) causes multi-system health concerns but not necessarily with prolonged QT. The disease can be recognized by any CACNA1C change (excluding the G406R change) that causes multi-system health concerns. Finding site True Cardiac conducting system structure Inferred relationship Some 3
A rare, multiple congenital anomalies syndrome with cardiac involvement as a major feature characterized by QT prolongation, congenital heart defects, syndactyly, facial dysmorphism and neurodevelopmental features. There are three clinical phenotypes recognized, the classical types that present with a prolonged QT interval and either with (TS1) or without (TS2) cutaneous syndactyly of fingers and toes. The atypical form (ATS) causes multi-system health concerns but not necessarily with prolonged QT. Finding site True Cardiac conducting system structure Inferred relationship Some 3
Postoperative cardiac arrhythmia Finding site True Cardiac conducting system structure Inferred relationship Some 2
Withdrawal arrhythmia Finding site True Cardiac conducting system structure Inferred relationship Some 1
Neonatal cardiac arrest Finding site True Cardiac conducting system structure Inferred relationship Some 2
Fetal cardiac arrest Finding site True Cardiac conducting system structure Inferred relationship Some 2
Cardiac arrest during cardiac surgery (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1
Cardiac arrhythmia during pregnancy (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 2
Stable tachyarrhythmia Finding site True Cardiac conducting system structure Inferred relationship Some 2
Stable bradyarrhythmia (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 2
Postural orthostatic tachycardia syndrome (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 3
A rare, genetic, primary orthostatic disorder characterized by dizziness, palpitations, fatigue, blurred vision and tachycardia following postural change from a supine to an upright position, in the absence of hypotension. A syncope with transient cognitive impairment and dyspnea may also occur. The norepinephrine transporter deficiency leads to abnormal uptake and high plasma concentrations of norepinephrine. Finding site True Cardiac conducting system structure Inferred relationship Some 2
Bier anemic spots, cyanosis, and urticaria-like eruption syndrome (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 3
Cardiac arrest following obstetric procedure (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 2
Persistent tachycardia during pregnancy (disorder) Finding site True Cardiac conducting system structure Inferred relationship Some 1

Start Previous Page 6 of 6

Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

Back to Start