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28882002: Disorder of sulfur-bearing amino acid metabolism (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
48363014 Disorder of sulphur-bearing amino acid metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
48366018 Disorder of transsulfuration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
48367010 Sulfuraminoacidemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484002019 Disorder of sulfur-bearing amino acid metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484003012 Disorder of transsulphuration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484004018 Sulphuraminoacidaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484005017 Disorder of sulphur-bearing amino acid including those due to folate and B12 disturbance en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
484006016 Disorder of sulfur-bearing amino acid including those due to folate and B12 disturbance en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
759612010 Disorder of sulfur-bearing amino acid metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
48363014 Disorder of sulphur-bearing amino acid metabolism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
48363014 Disorder of sulphur-bearing amino acid metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
48366018 Disorder of transsulfuration en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
48366018 Disorder of transsulfuration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
48367010 Sulfuraminoacidemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
48367010 Sulfuraminoacidemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484002019 Disorder of sulfur-bearing amino acid metabolism en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
484002019 Disorder of sulfur-bearing amino acid metabolism en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484003012 Disorder of transsulphuration en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
484003012 Disorder of transsulphuration en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484004018 Sulphuraminoacidaemia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
484004018 Sulphuraminoacidaemia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
484005017 Disorder of sulphur-bearing amino acid including those due to folate and B12 disturbance en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
484006016 Disorder of sulfur-bearing amino acid including those due to folate and B12 disturbance en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
759612010 Disorder of sulfur-bearing amino acid metabolism (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
759612010 Disorder of sulfur-bearing amino acid metabolism (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4482881000241118 trouble du métabolisme des acides aminés soufrés fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
4482881000241118 trouble du métabolisme des acides aminés soufrés fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

37 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of sulphur-bearing amino acid metabolism Is a Disorder of amino acid metabolism (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of sulphur-bearing amino acid metabolism Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of sulphur-bearing amino acid metabolism Finding site Body system structure false Inferred relationship Existential restriction modifier (core metadata concept)
Disorder of sulphur-bearing amino acid metabolism Is a Disorder of amino acid and organic acid metabolism true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Selective malabsorption of cyanocobalamin Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Methionine malabsorption syndrome Is a False Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Transcobalamin I deficiency Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Transcobalamin II deficiency (disorder) Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Homocystinuria Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Deficiency of dihydrofolate reductase (disorder) Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Cystathioninuria Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Functional defects of methionine synthase Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Cystathione gamma-lyase deficiency Is a False Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Sulfite oxidase deficiency Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
4-Hydroxyphenylpyruvate dioxygenase deficiency Is a False Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Sulphite oxidase deficiency syndrome Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
5,10-Methylenetetrahydrofolate reductase deficiency Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Hypermethioninaemia Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Familial methionine malabsorption Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Homocystinemia Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Glutamate formiminotransferase deficiency (disorder) Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Congenital defect of folate absorption (disorder) Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Cystathioninemia Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Cystathionine gamma-lyase deficiency Is a False Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Tetrahydrofolate methyltransferase deficiency (disorder) Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Cystathioninemia Is a False Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Other specified disturbance of sulfur-bearing amino acid metabolism Is a False Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Disturbance of sulfur-bearing amino acid metabolism NOS Is a False Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Cystathionine beta-synthase deficiency (disorder) Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Hawkinsinuria (disorder) Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Hyperhomocysteinemia (disorder) Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Beta-mercaptolactate cysteine disulfiduria (disorder) Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive extra-oral halitosis Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)
Developmental delay, immunodeficiency, leucoencephalopathy, hypohomocysteinemia syndrome Is a True Disorder of sulphur-bearing amino acid metabolism Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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