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398680004: Citrullinemia (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1766599016 Citrullinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1773235018 Citrullinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1774521013 Citrullinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1766599016 Citrullinemia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1766599016 Citrullinemia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1773235018 Citrullinaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1773235018 Citrullinaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1774521013 Citrullinemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1774521013 Citrullinemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786524014 Argininosuccinate synthase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786524014 Argininosuccinate synthase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786525010 ASS deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786526011 ASA synthase deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786527019 Argininosuccinase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786527019 Argininosuccinase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1786528012 ASAS deficiency en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1786529016 Arginosuccinate synthetase deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1786529016 Arginosuccinate synthetase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3438691001000117 Zitrullinämie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
85051000077110 citrullinémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
85051000077110 citrullinémie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3438691001000117 Zitrullinämie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

6 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Citrullinemia (disorder) Is a Enzymopathy true Inferred relationship Existential restriction modifier (core metadata concept)
Citrullinemia (disorder) Is a Aminoacidaemia true Inferred relationship Existential restriction modifier (core metadata concept)
Citrullinemia (disorder) Is a Disorder of the urea cycle metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Citrullinemia (disorder) Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Citrullinemia (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Citrullinemia (disorder) Is a Hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
Citrullinemia (disorder) Is a Hereditary metabolic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Citrullinemia (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Zitrullinämie, adulte, Typ 1 Is a False Citrullinemia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Citrullinemia, neonatal type (disorder) Is a True Citrullinemia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Citrullinemia, subacute type Is a True Citrullinemia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Citrin deficiency (disorder) Is a True Citrullinemia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)
Citrullinemia type I (disorder) Is a True Citrullinemia (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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