OMOP Concept 608081
Infantile glycine encephalopathy
StandardConditionSNOMED1156826003Disorder
Maps from
0
Descendants
1
Valid from
31 Jul 2021
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Synonyms
Alternative names recorded for Infantile glycine encephalopathy across source vocabularies.
- encefalopatía infantil por glicina
- encefalopatía infantil por glicina (trastorno)
- hiperglicinemia no cetósica infantil
- Infantile glycine encephalopathy (disorder)
- Infantile non-ketotic hyperglycinaemia
- Infantile non-ketotic hyperglycinemia
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
- 1Non-ketotic hyperglycinemia
- 2Autosomal hereditary disorder
- 2Hyperglycinemia
- 3Aminoacidemia
- 3Disorder of glycine metabolism
- 3Hereditary disease
- 4Acidemia
- 4Disorder of amino acid and organic acid metabolism
- 4Genetic disease
- 5Disease
- 5Disorder of acid-base balance
- 5Disorder of amino acid metabolism
- 6Clinical finding
- 6Disorder of organic acid metabolism
- 6Metabolic disease
Narrower concepts
(1)Included automatically when you query with descendants.
Get this concept via the API
Resolve Infantile glycine encephalopathy - and every code that maps to it - over HTTPS, against the current vocabulary release. No downloads, no local database.
curl "https://api.omophub.com/v1/concepts/608081?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card