OMOP Concept 37397546
Brunner syndrome
StandardConditionSNOMED718210003Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2016
Valid to
31 Dec 2099
OMOP concepts
Concept Lookup Tool
Search 11M+ concepts across SNOMED, RxNorm, ICD-10 & LOINC.
Source codes that map to this concept
1 source code normalizes to Brunner syndrome via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| MeSH | C563156 | Brunner Syndrome | Non-standard |
Synonyms
Alternative names recorded for Brunner syndrome across source vocabularies.
- deficiencia de monoamino oxidasa A
- deficiencia de monoamino oxidasa A (trastorno)
- Deficiency of monoamine oxidase A
- Deficiency of monoamine oxidase A (disorder)
- Monoamine oxidase A deficiency
- síndrome de Brunner
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(20)Roll up to these when you need a wider cohort.
- 1Deficiency of monoamine oxidase
- 1Inherited metabolic disorder of nervous system
- 1X-linked recessive hereditary disease
- 2Hereditary disorder of nervous system
- 2Inborn error of metabolism
- 2Specific enzyme deficiency
- 2X-linked hereditary disease
- 3Congenital disease
- 3Disorder of nervous system
- 3Enzymopathy
- 3Hereditary disorder by system
- 3Hereditary metabolic disease
- 3Sex-linked hereditary disorder
- 4Disorder of body system
- 4Fetal and/or neonatal disorder
- 4Hereditary disease
- 4Metabolic disease
- 5Disease
- 5Genetic disease
- 6Clinical finding
Get this concept via the API
Resolve Brunner syndrome - 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/37397546?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card