Timothy syndrome type 2 719907006
SNOMED CT code
| SNOMED code | 719907006 |
|---|---|
| name | Timothy syndrome type 2 |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Timothy syndrome type 2 (disorder) |
| synonyms | Timothy syndrome type 2 |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group3 | |
| Finding site | Cardiac conducting system structure 24964005 |
| attributes - group2 | |
| Finding site | Heart structure 80891009 |
| Occurrence | Congenital 255399007 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Timothy syndrome type 2 719907006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Timothy syndrome 1230096008 Timothy syndrome type 2 719907006 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Timothy syndrome type 2 719907006 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 Timothy syndrome type 2 719907006 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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