23501004: Arginase deficiency (disorder)

SNOMED CT Concept\Clinical finding\Disease\...

\Genetic disease\Hereditary disease\...

\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Arginase deficiency

\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Arginase deficiency

\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Arginase deficiency

\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Arginase deficiency
\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Inherited metabolic disorder of nervous system\Arginase deficiency

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Arginase deficiency
\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\Arginase deficiency
\Metabolic disease\Enzymopathy\Specific enzyme deficiency\Arginase deficiency

\Congenital disease\Inborn error of metabolism\Inherited metabolic disorder of nervous system\Arginase deficiency

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

39458015 Arginase deficiency en Synonym Active Entire term case insensitive SNOMED CT core module

39459011 Argininemia en Synonym Active Entire term case insensitive SNOMED CT core module

39460018 Hyperargininemia en Synonym Active Entire term case insensitive SNOMED CT core module

39461019 ARGI deficiency en Synonym Active Entire term case sensitive SNOMED CT core module

481635014 Argininaemia en Synonym Active Entire term case insensitive SNOMED CT core module

481636010 Hyperargininaemia en Synonym Active Entire term case insensitive SNOMED CT core module

753030010 Arginase deficiency (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

2475895017 Deficiency of arginase en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Arginase deficiency	Is a	Inherited metabolic disorder of nervous system	true	Inferred relationship	Existential restriction modifier
Arginase deficiency	Is a	Disorder of the urea cycle metabolism	true	Inferred relationship	Existential restriction modifier
Arginase deficiency	Is a	Enzymopathy	false	Inferred relationship	Existential restriction modifier
Arginase deficiency	Is a	Autosomal recessive hereditary disorder	true	Inferred relationship	Existential restriction modifier
Arginase deficiency	Finding site	Structure of nervous system	true	Inferred relationship	Existential restriction modifier	2
Arginase deficiency	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Arginase deficiency	Is a	Specific enzyme deficiency	true	Inferred relationship	Existential restriction modifier

Inbound Relationships

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This concept is not in any reference sets