OMOP Concept 37397477
Fatal infantile cytochrome C oxidase deficiency
StandardConditionSNOMED718124006Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Fatal infantile cytochrome C oxidase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 718124006 | Fatal infantile cytochrome C oxidase deficiency | Non-standard |
Synonyms
Alternative names recorded for Fatal infantile cytochrome C oxidase deficiency across source vocabularies.
- deficiencia infantil de oxidasa de citocromo C fatal
- deficiencia infantil de oxidasa de citocromo C fatal (trastorno)
- Fatal infantile cytochrome C oxidase deficiency (disorder)
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.
- 1Cytochrome-c oxidase deficiency
- 2Deficiency in enzyme complexes of mitochondrial respiratory chain
- 2Mitochondrial cytopathy
- 3Disorder of mitochondrial respiratory chain complexes
- 3Enzymopathy
- 3Metabolic disease
- 4Disease
- 4Disorder of pyruvate metabolism and mitochondrial respiratory chain
- 5Clinical finding
- 5Inborn error of metabolism
- 6Congenital disease
- 6Hereditary metabolic disease
- 7Disorder of fetus and/or newborn
- 7Hereditary disease
- 8Genetic disease
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