Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation 1204167003
SNOMED CT code
| SNOMED code | 1204167003 |
|---|---|
| name | Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation |
| status | active |
| date introduced | 2022-03-31 |
| fully specified name(s) | Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation (disorder) |
| synonyms | Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation |
| attributes - group2 | |
| Finding site | Ventricular conducting pathway 277943000 |
| attributes - group1 | |
| Interprets | Heart rate 364075005 |
| Has interpretation | Increased 35105006 |
| attributes - group3 | |
| Due to | Chromosomal disorder 409709004 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Cardiovascular finding 106063007 Cardiac finding 301095005 Heart disease 56265001 Cardiac complication 40172005 Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation 1204167003 SNOMED CT Concept 138875005 Clinical finding 404684003 Cardiovascular finding 106063007 Cardiac finding 301095005 Heart disease 56265001 Cardiac arrhythmia 698247007 Cardiac channelopathy 698271000 Catecholaminergic polymorphic ventricular tachycardia 419671004 Catecholaminergic polymorphic ventricular tachycardia due to calsequestrin mutation 1204167003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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