OMOP Concept 37167299
Late-onset citrullinemia type I
StandardConditionSNOMED1264112006Disorder
Maps from
0
Descendants
0
Valid from
28 Feb 2023
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Late-onset citrullinemia type I across source vocabularies.
- citrulinemia tipo 1 de inicio tardío
- citrulinemia tipo I de inicio tardío
- citrulinemia tipo I de inicio tardío (trastorno)
- Late-onset citrullinaemia type 1
- Late-onset citrullinaemia type I
- Late-onset citrullinemia type 1
- Late-onset citrullinemia type I (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(18)Roll up to these when you need a wider cohort.
- 1Citrullinemia type I
- 2Citrullinemia
- 3Aminoacidemia
- 3Autosomal recessive hereditary disorder
- 3Disorder of the urea cycle metabolism
- 3Enzymopathy
- 3Hereditary metabolic disease
- 4Acidemia
- 4Autosomal hereditary disorder
- 4Disorder of amino acid and organic acid metabolism
- 4Hereditary disease
- 4Metabolic disease
- 5Disease
- 5Disorder of acid-base balance
- 5Disorder of amino acid metabolism
- 5Genetic disease
- 6Clinical finding
- 6Disorder of organic acid metabolism
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