1388705009: Acute neonatal citrullinemia type I (disorder)

• SNOMED CT Concept\Clinical finding (finding)\...
• \Neonatal finding (finding)\Neonatal disorder\Neonatal metabolic disorder (disorder)\Acute neonatal citrullinemia type I (disorder)
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Citrullinemia (disorder)\Citrullinemia type I (disorder)\Acute neonatal citrullinemia type I (disorder)
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Citrullinemia (disorder)\Citrullinemia type I (disorder)\Acute neonatal citrullinemia type I (disorder)
• \Disease\Fetal and/or neonatal disorder\Neonatal disorder\Neonatal metabolic disorder (disorder)\Acute neonatal citrullinemia type I (disorder)
• \Disease\Metabolic disease\Hereditary metabolic disease\Citrullinemia (disorder)\Citrullinemia type I (disorder)\Acute neonatal citrullinemia type I (disorder)
• \Disease\Metabolic disease\Neonatal metabolic disorder (disorder)\Acute neonatal citrullinemia type I (disorder)
• \Disease\Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Aminoacidemia\Citrullinemia (disorder)\Citrullinemia type I (disorder)\Acute neonatal citrullinemia type I (disorder)
• \Disease\Metabolic disease\Disorder of organic acid metabolism\Disorder of amino acid metabolism\Disorder of amino acid and organic acid metabolism\Disorder of the urea cycle metabolism\Citrullinemia (disorder)\Citrullinemia type I (disorder)\Acute neonatal citrullinemia type I (disorder)
• \Disease\Metabolic disease\Enzymopathy\Citrullinemia (disorder)\Citrullinemia type I (disorder)\Acute neonatal citrullinemia type I (disorder)
• \Disease\Metabolic disease\Disorder of acid-base balance\Acidemia\Aminoacidemia\Citrullinemia (disorder)\Citrullinemia type I (disorder)\Acute neonatal citrullinemia type I (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 01-Mar 2026. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
6155085017	Acute neonatal citrullinemia type I (disorder)	en	Fully specified name	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6155086016	Acute neonatal citrullinaemia type 1	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6155087013	Early-onset citrullinaemia type I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6155088015	Early-onset citrullinaemia type 1	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6155089011	Acute neonatal citrullinaemia type I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6155090019	Acute neonatal citrullinemia type I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core
6155091015	Acute neonatal citrullinemia type 1	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6155092010	Early-onset citrullinemia type 1	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
6155093017	Early-onset citrullinemia type I	en	Synonym (core metadata concept)	Active	Only initial character case insensitive (core metadata concept)	SNOMED CT core

Expanded Value Set

This concept is not in any reference sets

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