Metabolic myopathy due to lactate transporter defect 766715000
SNOMED CT code
| SNOMED code | 766715000 |
|---|---|
| name | Metabolic myopathy due to lactate transporter defect |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Metabolic myopathy due to lactate transporter defect (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Finding site | Skeletal muscle structure 127954009 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Metabolic myopathy due to lactate transporter defect 766715000 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Metabolic myopathy 26111005 Metabolic myopathy due to lactate transporter defect 766715000 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Metabolic myopathy due to lactate transporter defect 766715000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Metabolic myopathy due to lactate transporter defect 766715000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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