Autosomal dominant myoglobinuria 725903003
SNOMED CT code
| SNOMED code | 725903003 |
|---|---|
| name | Autosomal dominant myoglobinuria |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Autosomal dominant myoglobinuria (disorder) |
| synonyms | Autosomal dominant myoglobinuria |
| attributes - group3 | |
| Has interpretation | Detected 260373001 |
| Interprets | Myoglobin measurement, urine 32375007 |
| attributes - group4 | |
| Occurrence | Congenital 255399007 |
| Finding site | Skeletal muscle structure 127954009 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Urine finding 301830001 Abnormal urinary product 106102002 Autosomal dominant myoglobinuria 725903003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Autosomal dominant myoglobinuria 725903003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Disorder of lysosomal enzyme 23585005 Lipid storage disease 10741005 Lipid storage myopathy 240095001 Autosomal dominant myoglobinuria 725903003 SNOMED CT Concept 138875005 Clinical finding 404684003 Musculoskeletal finding 106028002 Disorder of musculoskeletal system 928000 Hereditary disorder of musculoskeletal system 363212003 Autosomal dominant myoglobinuria 725903003 SNOMED CT Concept 138875005 Clinical finding 404684003 Urine finding 301830001 Finding of urine substance level 785672002 Myoglobinuria 48165008 Autosomal dominant myoglobinuria 725903003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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