Inclusion body myopathy 2 702382000
SNOMED CT code
| SNOMED code | 702382000 |
|---|---|
| name | Inclusion body myopathy 2 |
| status | active |
| date introduced | 2014-07-31 |
| fully specified name(s) | Inclusion body myopathy 2 (disorder) |
| synonyms |
|
| attributes - group1 | |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| 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 Congenital anomaly of skeletal muscle 89886004 Myopathy with cytoplasmic inclusions 240086009 Inclusion body myopathy 2 702382000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Inclusion body myopathy 2 702382000 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Inclusion body myopathy 2 702382000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Inclusion body myopathy 2 702382000 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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