OMOP Concept 4272491
Ethanolaminosis
StandardConditionSNOMED64235006Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
3 source codes normalize to Ethanolaminosis via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C562651 | Ethanolaminosis | Non-standard |
| Nebraska Lexicon | 64235006 | Ethanolamine kinase deficiency | Non-standard |
| Read | C30y100 | Ethanolaminuria | Non-standard |
Synonyms
Alternative names recorded for Ethanolaminosis across source vocabularies.
- deficiencia de etanolamina cinasa
- deficiencia de etanolamina quinasa
- etanolaminosis
- etanolaminosis (trastorno)
- etanolaminuria
- Ethanolamine kinase deficiency
- Ethanolaminosis (disorder)
- Ethanolaminuria
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.
- 1Autosomal recessive hereditary disorder
- 1Disorder of amino acid and organic acid metabolism
- 1Enzymopathy
- 1Inborn error of metabolism
- 2Autosomal hereditary disorder
- 2Congenital disease
- 2Disorder of amino acid metabolism
- 2Hereditary metabolic disease
- 2Metabolic disease
- 3Disease
- 3Disorder of fetus and/or newborn
- 3Disorder of organic acid metabolism
- 3Hereditary disease
- 4Clinical finding
- 4Genetic disease
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