OMOP Concept 4263710
Secondary myopathy
StandardConditionSNOMED60738003Disorder
Maps from
13
Descendants
392
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
13 source codes normalize to Secondary myopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 113072 | Secondary myopathy | Non-standard |
| CIM10 | G73.4 | Myopathy in infectious and parasitic diseases classified elsewhere | Non-standard |
| CIM10 | G73.7 | Myopathy in other diseases classified elsewhere | Non-standard |
| ICD10 | G73.4 | Myopathy in infectious and parasitic diseases classified elsewhere | Non-standard |
| ICD10 | G73.7 | Myopathy in other diseases classified elsewhere | Non-standard |
| ICD10CM | G73.7 | Myopathy in diseases classified elsewhere | Non-standard |
| ICD10CN | G73.4 | Myopathy in infectious and parasitic diseases classified elsewhere | Non-standard |
| ICD10CN | G73.7 | Myopathy in other diseases classified elsewhere | Non-standard |
| ICD10GM | G73.4 | Myopathy in infectious and parasitic diseases classified elsewhere | Non-standard |
| ICD10GM | G73.7 | Myopathy in other diseases classified elsewhere | Non-standard |
| KCD7 | G73.4 | Myopathy in infectious and parasitic diseases classified elsewhere | Non-standard |
| KCD7 | G73.7 | Myopathy in other diseases classified elsewhere | Non-standard |
| Read | F396z00 | Symptomatic inflammatory myopathy in disease NOS | Non-standard |
Synonyms
Alternative names recorded for Secondary myopathy across source vocabularies.
- miopatía secundaria
- miopatía secundaria (trastorno)
- Secondary myopathy (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(392)Included automatically when you query with descendants.
- 1Allergic bronchospasm caused by dietary substance
- 1Anaerobic myonecrosis
- 1Anal sphincter tear
- 1Autoimmune myopathy
- 1Bronchospasm caused by drug
- 1Calcification of muscle due to adult dermatomyositis
- 1Calcification of muscle due to juvenile dermatomyositis
- 1Carcinomatous myopathic syndrome
- 1Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
- 1Congenital myasthenic syndrome with glycosylation defect due to ALG14 UDP-N-acetylglucosaminyltransferase subunit gene mutation
- 1Contracture of gastrocnemius muscle due to traumatic injury
- 1Crushing injury of muscle
- 1Deafness, encephaloneuropathy, obesity, valvulopathy syndrome
- 1Deep contusion of muscle
- 1Diaphragmatic hernia with gastroesophageal reflux disease
- 1Disorder of muscle graft
- 1Foreign body granuloma of muscle
- 1Glycogen storage disease due to lactate dehydrogenase deficiency
- 1Glycogen storage disease due to muscle beta-enolase deficiency
- 1Human immunodeficiency virus myopathy
- 1Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation
- 1Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome
- 1Incomplete closure of velopharyngeal apparatus due to cleft palate
- 1Ischemia of muscle due to traumatic injury
- 1Laceration of muscle
Showing 25 of 392. Retrieve the full set via the API.
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