OMOP Concept 4095278
Metabolic myopathy
StandardConditionSNOMED26111005Disorder
Maps from
8
Descendants
87
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
8 source codes normalize to Metabolic myopathy via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 134265 | Metabolic myopathy | Non-standard |
| CIM10 | G73.6 | Myopathy in metabolic diseases | Non-standard |
| ICD10 | G73.6 | Myopathy in metabolic diseases | Non-standard |
| ICD10CN | G73.6 | Myopathy in metabolic diseases | Non-standard |
| ICD10GM | G73.6 | Myopathy in metabolic diseases | Non-standard |
| KCD7 | G73.6 | Myopathy in metabolic diseases | Non-standard |
| Read | F398.00 | Myopathy in metabolic diseases | Non-standard |
| Read | Fyu8800 | [X]Myopathy in metabolic diseases classified elsewhere | Non-standard |
Synonyms
Alternative names recorded for Metabolic myopathy across source vocabularies.
- Metabolic myopathy (disorder)
- miopatía metabólica
- miopatía metabólica (trastorno)
- Myopathy in metabolic diseases
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(10)Roll up to these when you need a wider cohort.
Narrower concepts
(87)Included automatically when you query with descendants.
- 1Chronic myopathy with hypocalcemia and hypophosphatemia
- 1Endocrine myopathy
- 1Familial periodic paralysis
- 1Glycogen storage disease, muscular form
- 1Lipid storage myopathy
- 1Metabolic myopathy due to lactate transporter defect
- 1Mitochondrial myopathy
- 1Muscle AMP deaminase deficiency
- 1Muscle and heart glycogen synthase deficiency
- 1Myopathy co-occurrent and due to hypercalcemia
- 1Nutritional myopathy
- 1Polyglucosan body myopathy type 1
- 1Polyglucosan body myopathy type 2
- 1Porcine stress syndrome
- 1Triglyceride deposit cardiomyovasculopathy
- 2Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy
- 2Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency
- 2Autosomal dominant mitochondrial myopathy with exercise intolerance
- 2Autosomal dominant myoglobinuria
- 2Childhood-onset spasticity with hyperglycinemia
- 2Combined oxidative phosphorylation defect type 39
- 2Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome
- 2Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome
- 2DNA2-related mitochondrial DNA deletion syndrome
- 2Equine polysaccharide storage myopathy
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