OMOP Concept 4224848
Andersen Tawil syndrome
StandardConditionSNOMED422348008Disorder
Maps from
2
Descendants
0
Valid from
31 Jul 2006
Valid to
31 Dec 2099
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Source codes that map to this concept
2 source codes normalize to Andersen Tawil syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | D050030 | Andersen Syndrome | Non-standard |
| Nebraska Lexicon | 422348008 | Andersen cardiodysrhythmic periodic paralysis | Non-standard |
Synonyms
Alternative names recorded for Andersen Tawil syndrome across source vocabularies.
- Andersen cardiodysrhythmic periodic paralysis
- Andersen Tawil syndrome (disorder)
- Long QT syndrome 7
- parálisis periódica cardiodisrítmica de Andersen
- síndrome de Andersen Tawil
- síndrome de Andersen Tawil (trastorno)
- síndrome de QT prolongado tipo 7
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(43)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Disorder of skeletal muscle
- 1Familial long QT syndrome
- 1Hereditary disorder of musculoskeletal system
- 1Movement disorder
- 1Periodic paralysis
- 2Autosomal hereditary disorder
- 2Cardiac arrhythmia associated with genetic disorder
- 2Cardiovascular system hereditary disorder
- 2Disease
- 2Disorder of muscle
- 2Disorder of musculoskeletal system
- 2Disorder of soft tissue
- 2Finding of movement
- 2Hereditary disorder by system
- 2Long QT syndrome
- 2Paralysis
- 3Cardiac arrhythmia
- 3Cardiac channelopathy
- 3Clinical finding
- 3Disorder of body system
- 3Disorder of cardiovascular system
- 3General finding of soft tissue
- 3Hereditary disease
- 3Motor dysfunction
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