OMOP Concept 4268626
Glycine dehydrogenase (decarboxylating) deficiency
StandardConditionSNOMED63329001Disorder
Maps from
1
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
1 source code normalizes to Glycine dehydrogenase (decarboxylating) deficiency via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 139372 | Glycine Dehydrogenase (Decarboxylating) Deficiency | Non-standard |
Synonyms
Alternative names recorded for Glycine dehydrogenase (decarboxylating) deficiency across source vocabularies.
- deficiencia de glicina descarboxilasa
- deficiencia de glicina deshidrogenasa (descarboxilante)
- deficiencia de glicina deshidrogenasa (descarboxilante) (trastorno)
- deficiencia de proteína P
- Glycine decarboxylase deficiency
- Glycine dehydrogenase decarboxylating deficiency
- Glycine dehydrogenase (decarboxylating) deficiency (disorder)
- hiperglicinemia no cetósica, tipo I
- Non-ketotic hyperglycinaemia P protein deficiency
- Non-ketotic hyperglycinaemia type I
- Nonketotic hyperglycinaemia, type I
- Non-ketotic hyperglycinemia P protein deficiency
- Non-ketotic hyperglycinemia type I
- Nonketotic hyperglycinemia, type I
- P protein deficiency
- P-protein deficiency
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Autosomal recessive hereditary disorder
- 1Enzymopathy
- 1Inborn error of metabolism
- 1Non-ketotic hyperglycinemia
- 2Autosomal hereditary disorder
- 2Congenital disease
- 2Hereditary metabolic disease
- 2Hyperglycinemia
- 2Metabolic disease
- 3Aminoacidemia
- 3Disease
- 3Disorder of glycine metabolism
- 3Fetal and/or neonatal disorder
- 3Hereditary disease
- 4Acidemia
- 4Clinical finding
- 4Disorder of amino acid and organic acid metabolism
- 4Genetic disease
- 5Disorder of acid-base balance
- 5Disorder of amino acid metabolism
- 6Disorder of organic acid metabolism
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