Myosclerosis 763895001
SNOMED CT code
| SNOMED code | 763895001 |
|---|---|
| name | Myosclerosis |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Myosclerosis (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Nervous system structure 25087005 |
| attributes - group1 | |
| Finding site | Skeletal muscle structure 127954009 |
| Occurrence | Congenital 255399007 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Myosclerosis 763895001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Myosclerosis 763895001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Myosclerosis 763895001 SNOMED CT Concept 138875005 Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Myosclerosis 763895001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Myosclerosis 763895001 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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