OMOP Concept 4163727
Propionic acidemia, type II
StandardConditionSNOMED399149003Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2003
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Propionic acidemia, type II via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 128367 | Propionic Acidemia, Type II | Non-standard |
Synonyms
Alternative names recorded for Propionic acidemia, type II across source vocabularies.
- acidemia propiónica tipo II
- acidemia propiónica tipo II (trastorno)
- Propionic acidaemia, type II
- Propionic acidemia, type II (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Propionic acidemia
- 2Acidemia
- 2Autosomal recessive hereditary disorder
- 2Disorder of branched-chain amino acid metabolism
- 2Disorder of propionate AND/OR methylmalonate metabolism
- 2Enzymopathy
- 2Inborn error of metabolism
- 2Non-amino organic acidemia AND/OR aciduria
- 3Autosomal hereditary disorder
- 3Congenital disease
- 3Disorder of acid-base balance
- 3Disorder of amino acid and organic acid metabolism
- 3Disorder of organic acid metabolism
- 3Hereditary metabolic disease
- 3Metabolic disease
- 4Disease
- 4Disorder of amino acid metabolism
- 4Fetal and/or neonatal disorder
- 4Hereditary disease
- 5Clinical finding
- 5Genetic disease
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