Benign congenital myopathy 193222002
SNOMED CT code
SNOMED code | 193222002 |
---|---|
name | Benign congenital myopathy |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Benign congenital myopathy (disorder) |
synonyms | Benign congenital myopathy |
attributes - group1 | |
Associated morphology | Morphologically abnormal structure 49755003 |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Skeletal muscle structure 127954009 |
parents | |
children | Benign Samaritan congenital myopathy 770787005 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Benign congenital myopathy 193222002 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Benign congenital myopathy 193222002 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 Benign congenital myopathy 193222002 |
ancestors | sorted most to least specific
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cpt crosswalks |
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