OMOP Concept 79804
Steinert myotonic dystrophy syndrome
StandardConditionSNOMED77956009Disorder
Maps from
5
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
5 source codes normalize to Steinert myotonic dystrophy syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| ICD10CM | G71.11 | Myotonic muscular dystrophy | Non-standard |
| Nebraska Lexicon | 77956009 | Dystrophia myotonica | Non-standard |
| OXMIS | 3309DM | DYSTROPHIA MYOTONICA | Non-standard |
| Read | F392000 | Dystrophia myotonica (Steinert's disease) | Non-standard |
| Read | F392011 | Steinert's disease | Non-standard |
Synonyms
Alternative names recorded for Steinert myotonic dystrophy syndrome across source vocabularies.
- distrofia miotónica tipo 1
- Myotonic dystrophy type 1
- síndrome de distrofia miotónica de Steinert
- síndrome de distrofia miotónica de Steinert (trastorno)
- síndrome de Steinert
- Steinert disease
- Steinert myotonic dystrophy syndrome (disorder)
- Steinert syndrome
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(27)Roll up to these when you need a wider cohort.
- 1Myotonic dystrophy
- 2Autosomal dominant hereditary disorder
- 2Hereditary progressive muscular dystrophy
- 2Myotonic disorder
- 3Autosomal hereditary disorder
- 3Developmental hereditary disorder
- 3Disorder of skeletal muscle
- 3Hereditary disorder of musculoskeletal system
- 3Muscular dystrophy
- 4Chronic disease of musculoskeletal system
- 4Degenerative disorder of muscle
- 4Degenerative disorder of musculoskeletal system
- 4Developmental disorder
- 4Disorder of muscle
- 4Disorder of musculoskeletal system
- 4Disorder of soft tissue
- 4Genetic disease
- 4Hereditary disease
- 4Hereditary disorder by system
- 5Chronic disease
- 5Degenerative disorder
- 5Disease
- 5Disorder of body system
- 5General finding of soft tissue
- 5Muscle finding
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