OMOP Concept 4178535
3-Methylglutaconic aciduria type 3
StandardConditionSNOMED297232009Disorder
Maps from
3
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
3 source codes normalize to 3-Methylglutaconic aciduria type 3 via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 159194 | Type III 3-methylglutaconic aciduria | Non-standard |
| MeSH | C535311 | Costeff optic atrophy syndrome | Non-standard |
| Nebraska Lexicon | 297232009 | 3-Methylglutaconic aciduria type 3 | Non-standard |
Synonyms
Alternative names recorded for 3-Methylglutaconic aciduria type 3 across source vocabularies.
- 3-Methylglutaconic aciduria type 3 (disorder)
- aciduria 3-metilglutacónica tipo 3
- aciduria 3-metilglutacónica tipo 3 (trastorno)
- Costeff syndrome
- síndrome de Costeff
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(12)Roll up to these when you need a wider cohort.
- 13-Methylglutaconic aciduria
- 1Autosomal recessive hereditary disorder
- 2Autosomal hereditary disorder
- 2Disorder of branched-chain amino acid metabolism
- 3Disorder of amino acid and organic acid metabolism
- 3Hereditary disease
- 4Disorder of amino acid metabolism
- 4Genetic disease
- 5Disease
- 5Disorder of organic acid metabolism
- 6Clinical finding
- 6Metabolic disease
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