Amyotrophia congenita 75491005
SNOMED CT code
| SNOMED code | 75491005 |
|---|---|
| name | Amyotrophia congenita |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Amyotrophia congenita (disorder) |
| synonyms | Amyotrophia congenita |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Skeletal muscle structure 127954009 |
| Associated morphology | Atrophy 13331008 |
| Occurrence | Congenital 255399007 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Hypoplasia 55199003 |
| 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 Hypoplasia of muscle 205530002 Amyotrophia congenita 75491005 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Degenerative disorder of muscle 363058009 Muscle atrophy 88092000 Amyotrophia congenita 75491005 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 Amyotrophia congenita 75491005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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