Hereditary coproporphyria 7425008
SNOMED CT code
| SNOMED code | 7425008 |
|---|---|
| name | Hereditary coproporphyria |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Hereditary coproporphyria (disorder) |
| synonyms |
|
| attributes - group1 | |
| Finding site | Liver structure 10200004 |
| parents | |
| children | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of porphyrin metabolism 29094004 Porphyria 418470004 Coproporphyria 190915002 Hereditary coproporphyria 7425008 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Hereditary coproporphyria 7425008 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Liver finding 249565005 Disease of liver 235856003 Hepatic porphyria 55056006 Hereditary coproporphyria 7425008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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