OMOP Concept 4131495
Non-amino organic acidemia AND/OR aciduria
StandardConditionSNOMED26513001Disorder
Maps from
2
Descendants
28
Valid from
31 Jan 2002
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
2 source codes normalize to Non-amino organic acidemia AND/OR aciduria via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 132942 | Non-Amino Organic Acidemia and/or Aciduria | Non-standard |
| HPO | HP_0001992 | Organic aciduria | Non-standard |
Synonyms
Alternative names recorded for Non-amino organic acidemia AND/OR aciduria across source vocabularies.
- acidemia y aciduria no amino orgánica
- acidemia Y/O aciduria no amino orgánica
- acidemia Y/O aciduria no amino orgánica (trastorno)
- Non-amino organic acidaemia AND/OR aciduria
- Non-amino organic acidemia AND/OR aciduria (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(4)Roll up to these when you need a wider cohort.
Narrower concepts
(28)Included automatically when you query with descendants.
- 1Acetyl-CoA carboxylase deficiency
- 1Glutaric aciduria
- 1Hydroxymethylglutaric aciduria
- 1Methylcrotonic aciduria
- 1Methylcrotonyl-CoA carboxylase deficiency
- 1Methylmalonic acidemia
- 1Propionic acidemia
- 2Adenosylcobalamin and methylcobalamin synthesis defect
- 2Adenosylcobalamin synthesis defect
- 2Combined malonic and methylmalonic aciduria
- 2Fatal infantile lactic acidosis with methylmalonic aciduria
- 2Glutaric aciduria, type 2
- 2Glutaryl-CoA dehydrogenase deficiency
- 2Methylmalonic acidemia due to methylmalonyl-coenzyme A epimerase deficiency
- 2Methylmalonic aciduria due to transcobalamin receptor defect
- 2Mitochondrial DNA depletion syndrome encephalomyopathic form with methylmalonic aciduria
- 2Propionic acidemia, type I
- 2Propionic acidemia, type II
- 2Propionyl-CoA carboxylase deficiency pccA complementation group
- 2Propionyl-CoA carboxylase deficiency pccBC complementation group
- 3Alpha chain electron transfer flavoprotein deficiency
- 3Beta chain electron transfer flavoprotein deficiency
- 3Cobalamin A disease
- 3Cobalamin B disease
- 3Cobalamin C disease
Showing 25 of 28. Retrieve the full set via the API.
Get this concept via the API
Resolve Non-amino organic acidemia AND/OR aciduria - 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/4131495?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card