OMOP Concept 37109462
Family history of Steinert myotonic dystrophy
StandardObservationSNOMED63931000119106Context-dependent
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Family history of Steinert myotonic dystrophy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 63931000119106 | Family history of myotonic muscular dystrophy | Non-standard |
Synonyms
Alternative names recorded for Family history of Steinert myotonic dystrophy across source vocabularies.
- antecedente familiar de distrofia miotónica de Steinert
- antecedente familiar de distrofia miotónica de Steinert (situación)
- Family history of myotonic muscular dystrophy
- Family history of Steinert myotonic dystrophy (situation)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Family history of hereditary disease
- 1FH: Muscular dystrophy
- 2Family history of chronic medical disorder
- 2Family history of development disorder
- 2Family history of disorder
- 2Family history of disorder of skeletal and/or smooth muscle
- 2FH: Musculoskeletal disease
- 2Have you or anyone in your family ever been diagnosed with the following brain and nervous system conditions? Think only of the people you are related to by blood. Select all that apply.
- 3Family history of clinical finding
- 3Family Members Diagnosed: Diagnosed Health Condition
- 3Have you or anyone in your family ever been diagnosed with the following bone, joint, and muscle conditions? Think only of the people you are related to by blood. Select all that apply.
- 4Family history with explicit context
- 4Finding with explicit context
- 5Family History
- 5Situation with explicit context
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