900000000000523009: POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept (foundation metadata concept)\Reference set\Association type\Historical association reference set (foundation metadata concept)\POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)

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

Descriptions:

Id Description Lang Type Status Case? Module

900000000001150016 POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

900000000001151017 POSSIBLY EQUIVALENT TO association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
Deer	Subfamily Cervinae (organism)
Deer fly bite allergen	Deer fly salivary protein (substance)
Deer mouse	Peromyscus maniculatus (organism)
Defaecation painful	Pain associated with defaecation
Defaecation painful	Pain associated with defaecation
Defaecation painful	Pain associated with defaecation
Defecation painful	Pain associated with defaecation
Defect	Abnormal communication
Defect	Absence (morphologic abnormality)
Defect	Morphologically abnormal structure
Defect of diaphragm	Diaphragmatic hernia
Defect of diaphragm	Disorder of diaphragm (disorder)
Defect of retina of bilateral eyes	Lesion of retina of bilateral eyes (disorder)
Defect of retina of bilateral eyes	Break of retina of bilateral eyes (disorder)
Defect of retina of left eye	Lesion of retina of left eye (disorder)
Defect of retina of left eye	Break of retina of left eye (disorder)
Defect of retina of right eye	Lesion of retina of right eye
Defect of retina of right eye	Break of retina of right eye (disorder)
Defective development of cauda equina	Congenital anomaly of cauda equina
Defective development of the cauda equina	Congenital anomaly of cauda equina
Deferoxamine mesylate 2g powder for injection solution vial	Deferoxamine mesilate 2 g powder for solution for injection vial
Deferoxamine mesylate 500mg injection	Deferoxamine mesilate 500 mg powder for solution for injection vial
Deferoxamine mesylate 500mg/vial injection	Deferoxamine mesilate 500 mg powder for solution for injection vial
Deferoxamine mesylate 500mg/vial powder	Deferoxamine mesilate 500 mg powder for solution for injection vial
Deferred	Delayed priority
Defibrination syndrome following abortive pregnancy	Induced termination of pregnancy complicated by defibrination syndrome (disorder)
Deficiencies of cell-mediated immunity	T-lymphocyte deficiency (finding)
Deficiencies of cell-mediated immunity	Cellular immune defect (finding)
Deficiencies of cell-mediated immunity	Predominantly T-cell defect (finding)
Deficiencies: [nutritional] or [vitamin]	Vitamin deficiency
Deficiency anaemiasm (& [asiderotic] or [sideropenic])	Iron deficiency anemia
Deficiency anaemiasm (& [asiderotic] or [sideropenic])	Deficiency anemias
Deficiency anemia associated with acquired immunodeficiency syndrome	Anaemia co-occurrent with human immunodeficiency virus infection
Deficiency of 4-hydroxyphenylpyruvate dioxygenase	Tyrosinemia type III (disorder)
Deficiency of 4-hydroxyphenylpyruvate dioxygenase	4-Hydroxyphenylpyruvate dioxygenase deficiency (disorder)
Deficiency of 4-hydroxyphenylpyruvate dioxygenase	Hawkinsinuria (disorder)
Deficiency of NAD^+^ nucleosidase	Deficiency of NAD^+^ nucleosidase
Deficiency of NAD^+^ nucleosidase	Deficiency of NADase
Deficiency of UTP-hexose-1-phosphate uridylyltransferase	Deficiency of UTP-hexose-1-phosphate uridylyltransferase
Deficiency of acetyl-CoA hydrolase	Deficiency of acetyl-CoA hydrolase
Deficiency of acetyl-CoA hydrolase	Deficiency of acetyl-CoA acylase
Deficiency of acetyl-CoA hydrolase	Deficiency of acetyl-CoA deacylase
Deficiency of acetylesterase	Deficiency of acetylesterase (disorder)
Deficiency of alkaline phosphatase	Deficiency of alkaline phosphatase
Deficiency of alkaline phosphatase	Deficiency of glycerophosphatase
Deficiency of alkaline phosphatase	Deficiency of alkaline phosphomonoesterase
Deficiency of alkaline phosphatase	Deficiency of phosphomonoesterase (disorder)
Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase	Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase
Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase	Deficiency of limit dextrinase
Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase	Glycogen storage disease type III
Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase	Deficiency of amylopectin 6-glucanohydrolase
Deficiency of amine oxidase	Deficiency of tyraminase
Deficiency of amine oxidase	Deficiency of amine oxidase
Deficiency of aminoacyl-histidine dipeptidase	Deficiency of carnosinase
Deficiency of aminoacyl-histidine dipeptidase	Deficiency of aminoacyl-histidine dipeptidase
Deficiency of aminopeptidase	Deficiency of peptidase a (disorder)
Deficiency of aminopeptidase	Deficiency of aminopeptidase
Deficiency of arylsulfatase	Deficiency of arylsulfatase
Deficiency of arylsulfatase	Deficiency of sulfatase
Deficiency of ascorbic acid	Ascorbic acid deficiency
Deficiency of ascorbic acid	Disorder of vitamin C (disorder)
Deficiency of cathepsin R	Deficiency of ribosomal cathepsin
Deficiency of cathepsin R	Deficiency of ribosomal neutral proteinase
Deficiency of cholinesterase	Deficiency of butyrylcholinesterase (disorder)
Deficiency of cholinesterase	Deficiency of acetylcholinesterase
Deficiency of cholinesterase	Deficiency of butyrylcholinesterase (disorder)
Deficiency of cholinesterase	Deficiency of acetylcholinesterase
Deficiency of chymotrypsin	Deficiency of chymotrypsin
Deficiency of chymotrypsin	Deficiency of chymotrypsin A and B
Deficiency of endopeptidase	Deficiency of endopeptidase
Deficiency of endopeptidase	Deficiency of protease
Deficiency of factor II &/or prothrombin	Factor II deficiency
Deficiency of gluconolactonase	Deficiency of aldonolactonase
Deficiency of gluconolactonase	Deficiency of gluconolactonase
Deficiency of gluconolactonase	Deficiency of lactonase
Deficiency of glycosidase	Deficiency of amylase
Deficiency of glycosidase	Deficiency of glycosidase
Deficiency of oligo-1,6-glucosidase	Deficiency of isomaltase
Deficiency of oligo-1,6-glucosidase	Sucrase-isomaltase deficiency
Deficiency of phosphoric monoester hydrolase	Deficiency of phosphatase
Deficiency of phosphoric monoester hydrolase	Deficiency of phosphoric monoester hydrolase
Deficiency of protein kinase	Deficiency of phosphorylase b kinase
Deficiency of protein kinase	Deficiency of protein kinase (disorder)
Deficiency of protein kinase	Deficiency of glycogen synthase a kinase (disorder)
Deficiency of protein kinase	Deficiency of hydroxyalkyl-protein kinase (disorder)
Deficiency of sulfuric ester hydrolase	Deficiency of sulphuric ester hydrolase
Deficiency of sulfuric ester hydrolase	Deficiency of sulfatase
Deficiency of trypsin	Deficiency of alpha- and beta-trypsin
Deficiency of trypsin	Deficiency of trypsin
Deficiency of vitamin A (disorder)	Vitamin A deficiency
Deficiency of vitamin A (disorder)	Disorder of vitamin A
Deficiency of vitamin B>12< (disorder)	Disorder of vitamin B12 (disorder)
Deficiency of vitamin B>12< (disorder)	Cobalamin deficiency
Deficiency of vitamin D (disorder)	Disorder of vitamin D (disorder)
Deficiency of vitamin D (disorder)	Vitamin D deficiency
Deficiency of vitamin D>2< (disorder)	Deficiency of vitamin D2 (disorder)
Deficiency of vitamin D>2< (disorder)	Disorder of vitamin D2 (disorder)
Deficiency of vitamin D>3< (disorder)	Disorder of vitamin D3 (disorder)
Deficiency of vitamin D>3< (disorder)	Deficiency of vitamin D3 (disorder)
Deficiency of vitamin K (disorder)	Disorder of vitamin K (disorder)
Deficiency of vitamin K (disorder)	Vitamin K deficiency

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Reference Sets

Reference set descriptor

Description inactivation indicator reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
900000000001150016	POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)	en	Fully specified name	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001151017	POSSIBLY EQUIVALENT TO association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)