OMOP Concept 37116747
3-phosphoglycerate dehydrogenase deficiency juvenile form
StandardConditionSNOMED733636005Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to 3-phosphoglycerate dehydrogenase deficiency juvenile form via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 733636005 | 3-phosphoglycerate dehydrogenase deficiency juvenile form | Non-standard |
Synonyms
Alternative names recorded for 3-phosphoglycerate dehydrogenase deficiency juvenile form across source vocabularies.
- 3-phosphoglycerate dehydrogenase deficiency juvenile form (disorder)
- forma juvenil de deficiencia de 3-fosfoglicerato deshidrogenasa
- forma juvenil de deficiencia de 3-fosfoglicerato deshidrogenasa (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(23)Roll up to these when you need a wider cohort.
- 13-Phosphoglycerate dehydrogenase deficiency
- 1Autosomal recessive hereditary disorder
- 1Disorder of the central nervous system
- 1Inherited metabolic disorder of nervous system
- 2Autosomal hereditary disorder
- 2Central nervous system finding
- 2Disorder of nervous system
- 2Disorder of serine metabolism
- 2Hereditary disorder of nervous system
- 2Inborn error of metabolism
- 3Clinical finding
- 3Congenital disease
- 3Disorder of amino acid and organic acid metabolism
- 3Disorder of body system
- 3Hereditary disease
- 3Hereditary disorder by system
- 3Hereditary metabolic disease
- 4Disease
- 4Disorder of amino acid metabolism
- 4Disorder of fetus and/or newborn
- 4Genetic disease
- 4Metabolic disease
- 5Disorder of organic acid metabolism
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