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373905003: Jervell and Lange-Nielsen syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
1229296017 Jervell and Lange-Nielsen syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
1229297014 Cardio-auditory syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
2971264016 Jervell and Lange-Nielsen syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Jervell and Lange-Nielsen syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Is a Congenital heart disease true Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Is a Conduction disorder of the heart false Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Is a Cardiovascular system hereditary disorder false Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Is a Congenital anomaly of ear with impairment of hearing false Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Associated morphology Congenital impairment false Inferred relationship Existential restriction modifier 2
Jervell and Lange-Nielsen syndrome Finding site Ear structure false Inferred relationship Existential restriction modifier 2
Jervell and Lange-Nielsen syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Finding site Structure of cardiovascular system false Inferred relationship Existential restriction modifier 2
Jervell and Lange-Nielsen syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Jervell and Lange-Nielsen syndrome Finding site Cardiac conducting system structure true Inferred relationship Existential restriction modifier 1
Jervell and Lange-Nielsen syndrome Is a Congenital conduction defect true Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Jervell and Lange-Nielsen syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Jervell and Lange-Nielsen syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Jervell and Lange-Nielsen syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Jervell and Lange-Nielsen syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Jervell and Lange-Nielsen syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Jervell and Lange-Nielsen syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Jervell and Lange-Nielsen syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Jervell and Lange-Nielsen syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Jervell and Lange-Nielsen syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Jervell and Lange-Nielsen syndrome Is a Congenital long QT syndrome true Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Is a Long QT syndrome with genetic marker false Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Jervell and Lange-Nielsen syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Jervell and Lange-Nielsen syndrome Finding site Ear structure false Inferred relationship Existential restriction modifier 3
Jervell and Lange-Nielsen syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Jervell and Lange-Nielsen syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 4
Jervell and Lange-Nielsen syndrome Finding site Cardiac conducting system structure false Inferred relationship Existential restriction modifier 4
Jervell and Lange-Nielsen syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 4
Jervell and Lange-Nielsen syndrome Interprets Functional observable false Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Is a Structural disorder of heart false Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Jervell and Lange-Nielsen syndrome Finding site Cardiac conducting system structure false Inferred relationship Existential restriction modifier 2
Jervell and Lange-Nielsen syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 3
Jervell and Lange-Nielsen syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Jervell and Lange-Nielsen syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 3
Jervell and Lange-Nielsen syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Jervell and Lange-Nielsen syndrome Is a Congenital sensorineural hearing loss true Inferred relationship Existential restriction modifier
Jervell and Lange-Nielsen syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Jervell and Lange-Nielsen syndrome Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 2
Jervell and Lange-Nielsen syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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