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373905003: Jervell and Lange-Nielsen syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
1229296017 Jervell and Lange-Nielsen syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1229297014 Cardio-auditory syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2971264016 Jervell and Lange-Nielsen syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1199205018 Jervell and Lange-Nielson syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1199205018 Jervell and Lange-Nielson syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
1212348017 Jervell and Lange-Nielson syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1212348017 Jervell and Lange-Nielson syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1229296017 Jervell and Lange-Nielsen syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1229296017 Jervell and Lange-Nielsen syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1229297014 Cardio-auditory syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1229297014 Cardio-auditory syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
2971264016 Jervell and Lange-Nielsen syndrome (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3393481001000112 Jervell-Lange-Nielsen-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
932291000172112 syndrome de Jervell et Lange-Nielsen fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
954361000172117 syndrome de long QT-surdité fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
932291000172112 syndrome de Jervell et Lange-Nielsen fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
954361000172117 syndrome de long QT-surdité fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3393481001000112 Jervell-Lange-Nielsen-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Jervell and Lange-Nielsen syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Is a Congenital heart disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Is a Conduction disorder of the heart false Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Is a Cardiovascular system hereditary disorder false Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Is a Congenital anomaly of ear with impairment of hearing false Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology Congenital impairment false Inferred relationship Existential restriction modifier (core metadata concept) 2
Jervell and Lange-Nielsen syndrome (disorder) Finding site Ear structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Jervell and Lange-Nielsen syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Finding site Structure of cardiovascular system (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Jervell and Lange-Nielsen syndrome (disorder) Finding site Cardiac conducting system structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Jervell and Lange-Nielsen syndrome (disorder) Is a Congenital conduction defect true Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 2
Jervell and Lange-Nielsen syndrome (disorder) Is a Familial long QT syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Is a Long QT syndrome with genetic marker false Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 3
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Jervell and Lange-Nielsen syndrome (disorder) Finding site Ear structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Jervell and Lange-Nielsen syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 4
Jervell and Lange-Nielsen syndrome (disorder) Finding site Cardiac conducting system structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Jervell and Lange-Nielsen syndrome (disorder) Interprets Hearing true Inferred relationship Existential restriction modifier (core metadata concept) 4
Jervell and Lange-Nielsen syndrome (disorder) Interprets entité observable fonctionnelle false Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Is a Structural disorder of heart false Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Jervell and Lange-Nielsen syndrome (disorder) Finding site Cardiac conducting system structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 3
Jervell and Lange-Nielsen syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Jervell and Lange-Nielsen syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Jervell and Lange-Nielsen syndrome (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Jervell and Lange-Nielsen syndrome (disorder) Is a Congenital sensorineural hearing loss (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Jervell and Lange-Nielsen syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Jervell and Lange-Nielsen syndrome (disorder) Finding site Structure of auditory system (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Jervell and Lange-Nielsen syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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