Neutral lipid storage disease with myopathy 699315005
SNOMED CT code
| SNOMED code | 699315005 |
|---|---|
| name | Neutral lipid storage disease with myopathy |
| status | active |
| date introduced | 2014-01-31 |
| fully specified name(s) | Neutral lipid storage disease with myopathy (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| attributes - group1 | |
| Finding site | Skeletal muscle structure 127954009 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Disorder of lysosomal enzyme 23585005 Lipid storage disease 10741005 Lipid storage myopathy 240095001 Neutral lipid storage disease with myopathy 699315005 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Neutral lipid storage disease with myopathy 699315005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Neutral lipid storage disease with myopathy 699315005 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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