Jervell and Lange-Nielsen syndrome 373905003
SNOMED CT code
| SNOMED code | 373905003 |
|---|---|
| name | Jervell and Lange-Nielsen syndrome |
| status | active |
| date introduced | 2002-07-31 |
| fully specified name(s) | Jervell and Lange-Nielsen syndrome (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Finding site | Cardiac conducting system structure 24964005 |
| attributes - group2 | |
| Finding site | Auditory structure 91159003 |
| Occurrence | Congenital 255399007 |
| attributes - group4 | |
| Interprets | Hearing 47078008 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Cardiovascular finding 106063007 Cardiac finding 301095005 Heart disease 56265001 Structural disorder of heart 128599005 Congenital heart disease 13213009 Jervell and Lange-Nielsen syndrome 373905003 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Congenital cardiovascular disorder 762228008 Congenital conduction defect 315027009 Jervell and Lange-Nielsen syndrome 373905003 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Jervell and Lange-Nielsen syndrome 373905003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Jervell and Lange-Nielsen syndrome 373905003 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Disorder of cardiovascular system 49601007 Cardiovascular system hereditary disorder 363005004 Familial long QT syndrome 442917000 Jervell and Lange-Nielsen syndrome 373905003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital sensorineural hearing loss 700453005 Jervell and Lange-Nielsen syndrome 373905003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Jervell and Lange-Nielsen syndrome 373905003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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