Proximal myopathy with extrapyramidal signs 770722002
SNOMED CT code
| SNOMED code | 770722002 |
|---|---|
| name | Proximal myopathy with extrapyramidal signs |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Proximal myopathy with extrapyramidal signs (disorder) |
| synonyms | Proximal myopathy with extrapyramidal signs |
| attributes - group3 | |
| Interprets | Movement 255324009 |
| attributes - group2 | |
| Finding site | Extrapyramidal system structure 76375004 |
| attributes - group1 | |
| Finding site | Skeletal muscle structure 127954009 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Proximal myopathy 193255007 Proximal myopathy with extrapyramidal signs 770722002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Proximal myopathy with extrapyramidal signs 770722002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Proximal myopathy with extrapyramidal signs 770722002 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of movement 298325004 Movement disorder 60342002 Extrapyramidal disease 76349003 Proximal myopathy with extrapyramidal signs 770722002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Proximal myopathy with extrapyramidal signs 770722002 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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