OMOP Concept 35608648
Familial benign copper deficiency
StandardConditionSNOMED763531001Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2018
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Familial benign copper deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C535468 | Copper deficiency, familial benign | Non-standard |
Synonyms
Alternative names recorded for Familial benign copper deficiency across source vocabularies.
- deficiencia familiar benigna de cobre
- deficiencia familiar benigna de cobre (trastorno)
- Familial benign copper deficiency (disorder)
- Familial benign hypocupraemia
- Familial benign hypocupremia
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(15)Roll up to these when you need a wider cohort.
- 1Disorder of copper metabolism
- 1Familial disease
- 1Hereditary metabolic disease
- 1Hypocupremia
- 2Disease
- 2Disorder of mineral metabolism
- 2Hereditary disease
- 2Metabolic disease
- 2Mineral deficiency
- 3Clinical finding
- 3Deficiency of micronutrients
- 3Genetic disease
- 4Undernutrition
- 5Nutritional deficiency disorder
- 6Nutritional disorder
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