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315027009: Congenital conduction defect (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
459490018 Congenital conduction defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
711876016 Congenital conduction defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5215481000241117 défaut de conduction congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


5 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital conduction defect Is a Congenital heart disease false Inferred relationship Some
Congenital conduction defect Associated morphology anomalie congénitale false Inferred relationship Some 1
Congenital conduction defect Finding site Structure of cardiovascular system subdivision (body structure) false Inferred relationship Some 2
Congenital conduction defect Finding site Heart structure false Inferred relationship Some
Congenital conduction defect Occurrence Congenital false Inferred relationship Some
Congenital conduction defect Finding site Structure of cardiovascular system (body structure) false Inferred relationship Some 2
Congenital conduction defect Finding site Intrathoracic cardiovascular structure false Inferred relationship Some
Congenital conduction defect Finding site Cardiac structure false Inferred relationship Some
Congenital conduction defect Is a Structural disorder of heart (disorder) false Inferred relationship Some
Congenital conduction defect Is a Any abnormal alteration of atrioventricular conduction. true Inferred relationship Some
Congenital conduction defect Finding site Cardiac conducting system structure false Inferred relationship Some 1
Congenital conduction defect Is a Congenital anomaly of cardiovascular system false Inferred relationship Some
Congenital conduction defect Is a Congenital anomaly of trunk false Inferred relationship Some
Congenital conduction defect Finding site Cardiac conducting system structure true Inferred relationship Some 1
Congenital conduction defect Associated morphology anomalie congénitale false Inferred relationship Some 1
Congenital conduction defect Is a Congenital disease false Inferred relationship Some
Congenital conduction defect Occurrence Congenital false Inferred relationship Some 2
Congenital conduction defect Finding site Cardiac conducting system structure false Inferred relationship Some 2
Congenital conduction defect Associated morphology anomalie du développement false Inferred relationship Some 2
Congenital conduction defect Occurrence Congenital true Inferred relationship Some 1
Congenital conduction defect Is a Congenital cardiovascular disorder (disorder) true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Jervell and Lange-Nielsen syndrome Is a True Congenital conduction defect Inferred relationship Some
Congenital heart block Is a True Congenital conduction defect Inferred relationship Some
Jervell and Lange-Nielson syndrome Is a False Congenital conduction defect Inferred relationship Some
Congenital complete atrioventricular heart block Is a True Congenital conduction defect Inferred relationship Some
Congenital incomplete atrioventricular heart block Is a True Congenital conduction defect Inferred relationship Some
Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome is a rare, genetic congenital anomalies/dysmorphic syndrome characterized by growth failure, global developmental delay, profound intellectual disability, autistic behaviors, acquired second-degree heart block with bradycardia and vasomotor instability. Hands and feet present with long fusiform fingers, campto-clinodactyly and crowded toes while craniofacial dysmorphism includes microcephaly, broad forehead, thin eyebrows, upslanting palpebral fissures, large ears with prominent antihelix, prominent nose, long philtrum, thin upper lip vermillion and prominent lower lip. Neurological signs include hypotonia, brisk reflexes, dystonic-like movements and truncal ataxia and imaging shows cerebellar hypoplasia and simplified gyral pattern. Is a True Congenital conduction defect Inferred relationship Some

This concept is not in any reference sets

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