Familial benign copper deficiency 763531001
SNOMED CT code
| SNOMED code | 763531001 |
|---|---|
| name | Familial benign copper deficiency |
| status | active |
| date introduced | 2018-07-31 |
| fully specified name(s) | Familial benign copper deficiency (disorder) |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Familial disease 111941005 Familial benign copper deficiency 763531001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Hereditary metabolic disease 1821000146108 Familial benign copper deficiency 763531001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Nutritional disorder 2492009 Nutritional deficiency disorder 70241007 Undernutrition 65404009 Deficiency of micronutrients 238111008 Mineral deficiency 111379007 Hypocupremia 19577007 Familial benign copper deficiency 763531001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of mineral metabolism 45744005 Disorder of copper metabolism 79886009 Familial benign copper deficiency 763531001 |
| ancestors | sorted most to least specific
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| cpt crosswalks |
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