Myotonic dystrophy 1177122009
SNOMED CT code
| SNOMED code | 1177122009 |
|---|---|
| name | Myotonic dystrophy |
| status | active |
| date introduced | 2021-10-31 |
| fully specified name(s) | Myotonic dystrophy (disorder) |
| synonyms |
|
| attributes - group2 | |
| Clinical course | Progressive 255314001 |
| attributes - group1 | |
| Finding site | Skeletal muscle structure 127954009 |
| Associated morphology | Dystrophy 4720007 |
| Pathological process | Pathological developmental process 308490002 |
| parents | |
| children | |
| 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 Myotonic dystrophy 1177122009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Hereditary progressive muscular dystrophy 193225000 Myotonic dystrophy 1177122009 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Myotonic disorder 193237003 Myotonic dystrophy 1177122009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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