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
Deep third degree burn of two OR more fingers not including thumb	Deep full thickness burn of finger (disorder)
Deep third degree burn of two OR more fingers not including thumb	Full thickness burn of skin and/or subcutaneous tissue of finger (disorder)
Deep third degree burn of upper arm with loss of body part	Deep third degree burn of upper arm
Deep third degree burn of upper limb with loss of body part	Deep third degree burn of upper arm
Deep third degree burn of wrist AND/OR hand	Deep third degree burn of wrist
Deep third degree burn of wrist AND/OR hand	Deep third degree burn of hand (disorder)
Deep third degree burn of wrist AND/OR hand with loss of body part	Deep third degree burn of wrist
Deep third degree burn of wrist AND/OR hand with loss of body part	Deep third degree burn of hand (disorder)
Deep third degree burn of wrist with loss of body part	Deep third degree burn of wrist
Deep third degree burns of multiple sites with loss of body part	Deep third degree burns of multiple sites (disorder)
Deep vein phlebitis and thrombophlebitis of the leg	Thrombophlebitis of deep veins of lower extremity
Deep vein phlebitis and thrombophlebitis of the leg NOS	Thrombophlebitis of deep veins of lower extremity
Deep vein thrombosis of leg related to intravenous drug use	Deep vein thrombosis of lower extremity due to intravenous drug use (disorder)
Deep vein thrombosis of lower limb	Deep venous thrombosis
Deep vein thrombosis of lower limb	Deep venous thrombosis of lower extremity (disorder)
Deep venous thrombosis of leg	Deep venous thrombosis of lower extremity (disorder)
Deep venous thrombosis of leg	Deep venous thrombosis
Deep venous thrombosis of lower extremity	Deep venous thrombosis
Deep venous thrombosis of lower extremity	Deep venous thrombosis of lower extremity (disorder)
Deep-tissue electromagnetic stimulation system, professional	Deep-tissue electromagnetic stimulation system
Deep-tissue electromagnetic stimulation system, professional/home-use	Deep-tissue electromagnetic stimulation system
Deer	Family Cervidae (organism)
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	Morphologically abnormal structure (morphologic abnormality)
Defect	Absence (morphologic abnormality)
Defect	Abnormal communication
Defect of diaphragm	Disorder of diaphragm (disorder)
Defect of diaphragm	Diaphragmatic hernia
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	Break of retina of right eye (disorder)
Defect of retina of right eye	Lesion of retina of right eye
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	Predominantly T-cell defect (finding)
Deficiencies of cell-mediated immunity	T-lymphocyte deficiency (finding)
Deficiencies of cell-mediated immunity	Cellular immune defect (finding)
Deficiencies: [nutritional] or [vitamin]	Vitamin deficiency (disorder)
Deficiency anaemiasm (& [asiderotic] or [sideropenic])	Deficiency anemias
Deficiency anaemiasm (& [asiderotic] or [sideropenic])	Iron deficiency anemia
Deficiency anemia associated with acquired immunodeficiency syndrome	Anaemia co-occurrent with human immunodeficiency virus infection
Deficiency of 4-hydroxyphenylpyruvate dioxygenase	4-Hydroxyphenylpyruvate dioxygenase deficiency (disorder)
Deficiency of 4-hydroxyphenylpyruvate dioxygenase	Hawkinsinuria (disorder)
Deficiency of 4-hydroxyphenylpyruvate dioxygenase	Tyrosinemia type III (disorder)
Deficiency of NAD^+^ nucleosidase	Deficiency of NADase
Deficiency of NAD^+^ nucleosidase	Deficiency of NAD^+^ nucleosidase
Deficiency of UTP-hexose-1-phosphate uridylyltransferase	Deficiency of UTP-hexose-1-phosphate uridylyltransferase
Deficiency of acetyl-CoA hydrolase	Deficiency of acetyl-CoA deacylase
Deficiency of acetyl-CoA hydrolase	Deficiency of acetyl-CoA acylase
Deficiency of acetyl-CoA hydrolase	Deficiency of acetyl-CoA hydrolase
Deficiency of acetylesterase	Deficiency of acetylesterase (disorder)
Deficiency of alkaline phosphatase	Deficiency of alkaline phosphomonoesterase
Deficiency of alkaline phosphatase	Deficiency of glycerophosphatase
Deficiency of alkaline phosphatase	Deficiency of phosphomonoesterase
Deficiency of alkaline phosphatase	Deficiency of alkaline phosphatase
Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase	Deficiency of amylopectin 6-glucanohydrolase
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 alpha-dextrin endo-1,6-alpha-glucosidase
Deficiency of alpha-dextrin endo-1,6-alpha-glucosidase	Deficiency of limit dextrinase
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 (disorder)
Deficiency of aminopeptidase	Deficiency of aminopeptidase
Deficiency of aminopeptidase	Deficiency of peptidase a
Deficiency of arylsulfatase	Deficiency of sulfatase
Deficiency of arylsulfatase	Deficiency of arylsulfatase
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 acetylcholinesterase
Deficiency of cholinesterase	Deficiency of butyrylcholinesterase (disorder)
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 lactonase
Deficiency of gluconolactonase	Deficiency of gluconolactonase
Deficiency of glycosidase	Deficiency of glycosidase
Deficiency of glycosidase	Deficiency of amylase
Deficiency of inosine nucleosidase	Deficiency of inosinase
Deficiency of inosine nucleosidase	Deficiency of inosine nucleosidase

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Reference Sets

Reference set descriptor

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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)