Congenital muscular dystrophy due to LMNA mutation 771272007
SNOMED CT code
| SNOMED code | 771272007 |
|---|---|
| name | Congenital muscular dystrophy due to LMNA mutation |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Congenital muscular dystrophy due to lamin A/C mutation (disorder) |
| synonyms |
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| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Dystrophy 4720007 |
| Occurrence | Congenital 255399007 |
| Finding site | Skeletal muscle structure 127954009 |
| attributes - group2 | |
| Clinical course | Progressive 255314001 |
| 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 Congenital hereditary muscular dystrophy 111501005 Congenital muscular dystrophy due to LMNA mutation 771272007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Congenital muscular dystrophy due to LMNA mutation 771272007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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