OMOP Concept 4274792
Sarcosine dehydrogenase deficiency
StandardConditionSNOMED64852002Disorder
Maps from
5
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
5 source codes normalize to Sarcosine dehydrogenase deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 127164 | Sarcosine dehydrogenase deficiency | Non-standard |
| HPO | HP_0010896 | Hypersarcosinemia | Non-standard |
| HPO | HP_0010897 | Hypersarcosinuria | Non-standard |
| MeSH | C537236 | Sarcosinemia | Non-standard |
| Read | C30y700 | Sarcosinaemia | Non-standard |
Synonyms
Alternative names recorded for Sarcosine dehydrogenase deficiency across source vocabularies.
- defecto de desmetilación de N - metilglicina
- deficiencia del complejo sarcosina deshidrogenasa
- deficiencia de sarcosina deshidrogenasa
- deficiencia de sarcosina deshidrogenasa (trastorno)
- Deficiency of the sarcosine dehydrogenase complex
- Demethylation defect of N-methylglycine
- hipersarcosinemia
- Hypersarcosinaemia
- Hypersarcosinemia
- Sarcosinaemia
- Sarcosine dehydrogenase deficiency (disorder)
- sarcosinemia
- Sarcosinemia
- sarcosinuria
- Sarcosinuria
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Disorder of glycine metabolism
- 1Enzymopathy
- 1Inborn error of metabolism
- 2Autosomal hereditary disorder
- 2Congenital disease
- 2Disorder of amino acid and organic acid metabolism
- 2Hereditary metabolic disease
- 2Metabolic disease
- 3Disease
- 3Disorder of amino acid metabolism
- 3Fetal and/or neonatal disorder
- 3Hereditary disease
- 4Clinical finding
- 4Disorder of organic acid metabolism
- 4Genetic disease
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