OMOP Concept 436672
Disorder of copper metabolism
StandardConditionSNOMED79886009Disorder
Maps from
16
Descendants
13
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
16 source codes normalize to Disorder of copper metabolism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 142099 | Disorder of copper metabolism | Non-standard |
| CIM10 | E83.0 | Disorders of copper metabolism | Non-standard |
| ICD10 | E83.0 | Disorders of copper metabolism | Non-standard |
| ICD10CM | E83.0 | Disorders of copper metabolism | Non-standard |
| ICD10CM | E83.00 | Disorder of copper metabolism, unspecified | Non-standard |
| ICD10CM | E83.09 | Other disorders of copper metabolism | Non-standard |
| ICD10CN | E83.0 | Disorders of copper metabolism | Non-standard |
| ICD10CN | E83.000 | Disorders of copper metabolism | Non-standard |
| ICD10CN | E83.001 | Wilson's disease (machine translation) | Non-standard |
| ICD10CN | E83.002 | Menkes syndrome (machine translation) | Non-standard |
| ICD10GM | E83.0 | Disorders of copper metabolism | Non-standard |
| ICD9CM | 275.1 | Disorders of copper metabolism | Non-standard |
| KCD7 | E83.0 | Disorders of copper metabolism | Non-standard |
| Nebraska Lexicon | 79886009 | Disorder of copper metabolism | Non-standard |
| Read | C351.00 | Disorders of copper metabolism | Non-standard |
| Read | C351z00 | Disorder of copper metabolism NOS | Non-standard |
Synonyms
Alternative names recorded for Disorder of copper metabolism across source vocabularies.
- Copper metabolism disorder
- Disorder of copper metabolism (disorder)
- trastorno del metabolismo del cobre
- trastorno del metabolismo del cobre (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(13)Included automatically when you query with descendants.
- 1Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect
- 1Cutis laxa, x-linked
- 1Familial benign copper deficiency
- 1Familial hypoceruloplasminemia
- 1Hypercupruria
- 1Indian childhood cirrhosis
- 1Menkes kinky-hair syndrome
- 1Nutritional myelopathy of pigs
- 1Primary copper-associated hepatitis
- 1Swayback of sheep
- 1Wilson's disease
- 2Chorea co-occurrent and due to Wilson disease
- 2Westphal-Strumpell syndrome
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