Andersen Tawil syndrome 422348008
SNOMED CT code
| SNOMED code | 422348008 |
|---|---|
| name | Andersen Tawil syndrome |
| status | active |
| date introduced | 2006-07-31 |
| fully specified name(s) | Andersen Tawil syndrome (disorder) |
| synonyms |
|
| attributes - group4 | |
| Interprets | Movement 255324009 |
| attributes - group2 | |
| Finding site | Skeletal muscle structure 127954009 |
| attributes - group1 | |
| Interprets | Movement observable 363847004 |
| Has interpretation | Absent 2667000 |
| attributes - group3 | |
| Finding site | Cardiac conducting system structure 24964005 |
| 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 Andersen Tawil syndrome 422348008 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of movement 298325004 Motor dysfunction 52559000 Paralysis 44695005 Periodic paralysis 198030008 Andersen Tawil syndrome 422348008 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Andersen Tawil syndrome 422348008 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 Andersen Tawil syndrome 422348008 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of movement 298325004 Movement disorder 60342002 Andersen Tawil syndrome 422348008 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Andersen Tawil syndrome 422348008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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