OMOP Concept 36714285
Deficiency of dimethylglycine dehydrogenase
StandardConditionSNOMED719449007Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Deficiency of dimethylglycine dehydrogenase via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C565278 | Dimethylglycine Dehydrogenase Deficiency | Non-standard |
Synonyms
Alternative names recorded for Deficiency of dimethylglycine dehydrogenase across source vocabularies.
- deficiencia de dimetilglicina deshidrogenasa
- deficiencia de dimetilglicina deshidrogenasa (trastorno)
- Deficiency of dimethylglycine dehydrogenase (disorder)
- Dimethylglycine dehydrogenase deficiency
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(13)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Disorder of glycine metabolism
- 1Specific enzyme deficiency
- 2Autosomal hereditary disorder
- 2Disorder of amino acid and organic acid metabolism
- 2Enzymopathy
- 3Disorder of amino acid metabolism
- 3Hereditary disease
- 3Metabolic disease
- 4Disease
- 4Disorder of organic acid metabolism
- 4Genetic disease
- 5Clinical finding
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