Desmin-related myofibrillar myopathy 770627003
SNOMED CT code
| SNOMED code | 770627003 |
|---|---|
| name | Desmin-related myofibrillar myopathy |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Desmin-related myofibrillar myopathy (disorder) |
| synonyms |
|
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Skeletal muscle structure 127954009 |
| Occurrence | Congenital 255399007 |
| 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 Desmin-related myofibrillar myopathy 770627003 SNOMED CT Concept 138875005 Clinical 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 Desmin-related myofibrillar myopathy 770627003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Desmin-related myofibrillar myopathy 770627003 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Desmin-related myofibrillar myopathy 770627003 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Myofibrillar myopathy 699269005 Desmin-related myofibrillar myopathy 770627003 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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