OMOP Concept 4121882
Inborn errors of metabolism marker
StandardObservationSNOMED259357003Substance
Maps from
2
Descendants
42
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 Inborn errors of metabolism marker via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 259357003 | Inborn errors of metabolism marker | Non-standard |
| Nebraska Lexicon | 767280006 | Metabolic marker | Non-standard |
Synonyms
Alternative names recorded for Inborn errors of metabolism marker across source vocabularies.
- Inborn errors of metabolism marker (substance)
- marcador de metabolopatías congénitas
- marcador de metabolopatías congénitas (sustancia)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Narrower concepts
(42)Included automatically when you query with descendants.
- 1Amino acid metabolism disorder marker
- 1Carbohydrate metabolism disorder marker
- 1Glycoprotein and mucolipid storage disease marker
- 1Glycosaminoglycanoses marker
- 1Lactic acidemia and mitochondrial disorder marker
- 1Lipoprotein and neutral lipid disorder marker
- 1Lysosomal storage disease marker
- 1Mitochondrial adenosine triphosphate synthase subunit c
- 1Organic acid metabolism disorder marker
- 1Peroxisomal disorder marker
- 1Porphyrin and heme metabolism disorder marker
- 1Propionate and methylmalonate metabolism disorder marker
- 1Purine and pyrimidine metabolism disorder marker
- 1Steroid metabolism disorder marker
- 23-Hydroxymyristoleylcarnitine
- 2Acylglycine
- 2Asialo GM2
- 2Bifunctional enzyme
- 2Branched chain organic acid disorder marker
- 2Carbon (14-C) triolein
- 2Cerebroside sulfatase activator
- 2Cross-linked hyaluronan
- 2GM2-ganglioside activator protein
- 2Guanidinoacetic acid
- 2Ketone body
- 2Ornithine and lysine metabolism disorder marker
- 2p-coumaric acid
- 2Phenylalanine and tyrosine disorder marker
- 2Plasma membrane high affinity low density lipoprotein receptor
- 2Polysulfated glycosaminoglycan
- 2Purine and pyrimidine disorder marker enzyme
- 2Pyruvate dehydrogenase complex E1 alpha subunit
- 2Radioisotope labeled vitamin B12
- 2Sitosterol
- 2Sulfite salt
- 2Sulfur amino acid disorder markers
- 2Syndecan-1
- 2Urea cycle disorder marker
- 3Argininosuccinic acid
- 3Lysosomal cystine transport protein
- 3Melanogen
- 3Nicotinurate
Get this concept via the API
Resolve Inborn errors of metabolism marker - 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/4121882?include_relationships=true" \
-H "Authorization: Bearer $OMOPHUB_API_KEY"Get your free API key3,000 calls/month free · no credit card