OMOP Concept 4305951
Disorder of glycine metabolism
StandardConditionSNOMED83076007Disorder
Maps from
10
Descendants
14
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
10 source codes normalize to Disorder of glycine metabolism via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 142078 | Disorder of glycine metabolism | Non-standard |
| CIM10 | E72.5 | Disorders of glycine metabolism | Non-standard |
| ICD10 | E72.5 | Disorders of glycine metabolism | Non-standard |
| ICD10CM | E72.5 | Disorders of glycine metabolism | Non-standard |
| ICD10CM | E72.50 | Disorder of glycine metabolism, unspecified | Non-standard |
| ICD10CM | E72.59 | Other disorders of glycine metabolism | Non-standard |
| ICD10CN | E72.5 | Disorders of glycine metabolism | Non-standard |
| ICD10CN | E72.500 | Disorders of glycine metabolism | Non-standard |
| ICD10GM | E72.5 | Disorders of glycine metabolism | Non-standard |
| KCD7 | E72.5 | Disorders of glycine metabolism | Non-standard |
Synonyms
Alternative names recorded for Disorder of glycine metabolism across source vocabularies.
- Disorder of glycine metabolism (disorder)
- trastorno del metabolismo de la glicina
- trastorno del metabolismo de la glicina (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(6)Roll up to these when you need a wider cohort.
Narrower concepts
(14)Included automatically when you query with descendants.
- 1Deficiency of dimethylglycine dehydrogenase
- 1Glycinuria
- 1Hyperglycinemia
- 1Sarcosine dehydrogenase deficiency
- 2Non-ketotic hyperglycinemia
- 2Transient neonatal hyperglycinemia
- 3Aminomethyltransferase deficiency
- 3Atypical glycine encephalopathy
- 3Childhood-onset spasticity with hyperglycinemia
- 3Glycine dehydrogenase (decarboxylating) deficiency
- 3Infantile glycine encephalopathy
- 3Non-ketotic hyperglycinemia H protein deficiency
- 3Non-ketotic hyperglycinemia L protein deficiency
- 4Neonatal glycine encephalopathy
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