900000000000526001: REPLACED BY 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)\REPLACED BY 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

900000000001156010 REPLACED BY 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)
900000000001157018 REPLACED BY 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
REPLACED BY association reference set (foundation metadata concept)	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
Potassium chloride 15meq	Potassium chloride only product
kaliumklorid 15 milliekvivalenter per förpackning	Potassium chloride only product
kaliumklorid 1 000 mg/5 ml, lösning	Potassium chloride only product
kaliumklorid 1 000 mg/ml, lösning	Product containing precisely potassium chloride 100 milligram/1 milliliter conventional release oral solution (clinical drug)
kaliumklorid 20 %, injektionsvätska, lösning, ampull	Potassium chloride 200 mg/mL solution for injection
kaliumklorid 20 %, lösning	Potassium chloride only product
kaliumklorid 20 milliekvivalenter, pulver	Product containing precisely potassium chloride 1.5 gram/1 sachet powder for conventional release oral solution (clinical drug)
Potassium chloride 20meq/15m solution	Product containing precisely potassium chloride 100 milligram/1 milliliter conventional release oral solution (clinical drug)
kaliumklorid 20 milliekvivalenter/15 ml, lösning	Product containing precisely potassium chloride 100 milligram/1 milliliter conventional release oral solution (clinical drug)
kaliumklorid 20 milliekvivalenter per förpackning	Potassium chloride only product
dextros 4 % + natriumklorid 0,18 % + kaliumklorid 20 mmol, infusionsvätska, lösning, påse 1 000 ml	Anhydrous glucose 40 mg/mL and potassium chloride 1.5 mg/mL and sodium chloride 1.8 mg/mL solution for injection
dextros 4 % + natriumklorid 0,18 % + kaliumklorid 20 mmol, infusionsvätska, lösning, påse 500 ml	Anhydrous glucose 40 mg/mL and potassium chloride 3 mg/mL and sodium chloride 1.8 mg/mL solution for injection
glukos 5 % + kaliumklorid 20 mmol, infusionsvätska, lösning, påse 1 000 ml	Anhydrous glucose 50 mg/mL and potassium chloride 1.5 mg/mL solution for injection
glukos 5 % + kaliumklorid 20 millimol, infusionsvätska, lösning, påse 500 ml	Anhydrous glucose 50 mg/mL and potassium chloride 3 mg/mL solution for injection
natriumklorid 0,9 % + kaliumklorid 20 mmol, infusionsvätska, lösning, påse 1 000 ml	Product containing precisely potassium chloride 1.5 milligram/1 milliliter and sodium chloride 9 milligram/1 milliliter conventional release solution for injection (clinical drug)
natriumklorid 0,9 % + kaliumklorid 20 mmol, infusionsvätska, lösning, påse 500 ml	Product containing precisely potassium chloride 3 milligram/1 milliliter and sodium chloride 9 milligram/1 milliliter conventional release solution for injection (clinical drug)
dextros 4 % + natriumklorid 0,18 % + kaliumklorid 27 mmol, infusionsvätska, lösning, påse 1 000 ml	Anhydrous glucose 40 mg/mL and potassium chloride 2 mg/mL and sodium chloride 1.8 mg/mL solution for injection
glukos 5 % + kaliumklorid 27 mmol, infusionsvätska, lösning, påse 1 000 ml	Anhydrous glucose 50 mg/mL and potassium chloride 2 mg/mL solution for injection
natriumklorid 0,9 % + kaliumklorid 27 mmol, infusionsvätska, lösning, påse 1000 ml	Product containing precisely potassium chloride 2 milligram/1 milliliter and sodium chloride 9 milligram/1 milliliter conventional release solution for injection (clinical drug)
dextros 4 % + natriumklorid 0,18 % + kaliumklorid 40 mmol, infusionsvätska, lösning, påse 1 000 ml	Anhydrous glucose 40 mg/mL and potassium chloride 3 mg/mL and sodium chloride 1.8 mg/mL solution for injection
glukos 5 % + kaliumklorid 40 mmol, infusionsvätska, lösning, påse 1 000 ml	Anhydrous glucose 50 mg/mL and potassium chloride 3 mg/mL solution for injection
natriumklorid 0,9 % + kaliumklorid 40 mmol, infusionsvätska, lösning, påse 1 000 ml	Product containing precisely potassium chloride 3 milligram/1 milliliter and sodium chloride 9 milligram/1 milliliter conventional release solution for injection (clinical drug)
kaliumklorid 7,5 %, sirap	Product containing only potassium chloride in oral dose form (medicinal product form)
injektionskoncentrat kaliumklorid 15 %, lösning, ampull	Product containing only potassium chloride in parenteral dose form (medicinal product form)
kaliumcitrat 12 g/10 ml koncentrerad blandning	Product containing only potassium citrate in oral dose form (medicinal product form)
kaliumcitrat 12 g/10 ml, oral lösning	Product containing only potassium citrate in oral dose form (medicinal product form)
kaliumcitrat 3 g/dospåse, granulat	Product containing only potassium citrate in oral dose form (medicinal product form)
biverkningar av kaliumklorazepat	Adverse reaction to clorazepate
kaliumglukonat 20 milliekvivalenter/15 ml, elixir	Product containing precisely potassium gluconate 312 milligram/1 milliliter conventional release oral solution (clinical drug)
kaliumpermanganat 400 mg, tablett till kutan lösning	Product containing permanganic acid in cutaneous dose form (medicinal product form)
kaliumpermanganat 400 mg, tablett till lösning	Product containing permanganic acid in cutaneous dose form (medicinal product form)
kaliumfosfat 2 mmol/ml, injektionsvätska, lösning, ampull 10 ml	Product containing precisely monobasic potassium phosphate 136 milligram/1 milliliter conventional release solution for injection (clinical drug)
kaliumtillskott	Potassium and/or potassium compound
potatis, livsmedel	Potato (substance)
potentiell exponering för infektion	Exposure to organism (event)
Potential infectious contact	Exposure to organism (event)
Potential infectious contact	Exposure to organism (event)
Potexvirus group	Genus Potexvirus (organism)
Potts fraktur	Bimalleolar fracture of ankle
Pouched mammal	Infraclass Metatheria (organism)
povidon 5 %, ögondroppar	Povidone 50 mg/mL eye solution
povidon 5 %, ögondroppar för engångsbruk	Povidone 50 mg/mL eye solution
joderad povidon 10 %	Product containing povidone iodine (medicinal product)
joderad povidon 10 %, preparat för pensling	Product containing precisely povidone iodine 100 milligram/1 milliliter conventional release cutaneous solution (clinical drug)
joderad povidon 10 %, svamp för lokalt bruk	Product containing precisely povidone iodine 100 milligram/1 milliliter conventional release cutaneous solution (clinical drug)
joderad povidon 10 %, vaginalgel	Iodine (as povidone iodine) 100 mg/g vaginal gel
joderad povidon 20 %, svamp för lokalt bruk	Povidone iodine only product in cutaneous dose form
joderad povidon 200 mg, suppositorium	Product containing precisely iodine (as povidone iodine) 200 milligram/1 each conventional release vaginal tablet (clinical drug)
joderad povidon 5 %, svamp för lokalt bruk	Product containing precisely povidone iodine 50 milligram/1 milliliter conventional release cutaneous solution (clinical drug)
pulver till instillationslösning för luftvägarna	Powder for solution for endotracheopulmonary instillation
pulver till suspension för endotrakeal instillation	Powder for conventional release suspension for endotracheopulmonary instillation (dose form)
pulver till suspension	Powder (basic dose form)
Powered wheelchair	Motorized wheelchair device (physical object)
Poxvirus group	Family Poxviridae (organism)
Pramipexole dihydrochloride 125micrograms tablet	Product containing precisely pramipexole (as pramipexole dihydrochloride) 88 microgram/1 each conventional release oral tablet (clinical drug)
Pramipexole dihydrochloride 1mg tablet	Pramipexole (as pramipexole dihydrochloride) 700 microgram oral tablet
Pramipexole dihydrochloride 250micrograms tablet	Pramipexole (as pramipexole dihydrochloride) 180 microgram oral tablet
pramlintid 1 mg/ml, injektionsvätska, lösning, förfylld penna	Pramlintide only product
Pre-excitation atrioventricular conduction	Accelerated atrioventricular conduction
befintlig terapi ändrad av anestesiolog preoperativt	Pre-existing therapy altered by anesthetist preoperatively (situation)
duplexvaccination mot difteri och stelkramp i förskoleåldern	Preschool administration of diphtheria and tetanus vaccine
Precautionary nursing procedure	Nursing procedure
Prediabetes	Impaired glucose tolerance
prednisolon 0,001 %, ögondroppar	Prednisolone (as prednisolone sodium phosphate) 10 microgram/mL eye solution
prednisolon 0,003 %, ögondroppar	Product containing precisely prednisolone (as prednisolone sodium phosphate) 30 microgram/1 milliliter conventional release eye solution (clinical drug)
prednisolon 0,01 %, ögondroppar	Prednisolone (as prednisolone sodium phosphate) 100 microgram/mL eye solution
prednisolon 0,01 %, ögondroppar	Prednisolone (as prednisolone sodium phosphate) 100 microgram/mL eye solution
prednisolon 0,01 %, ögondroppar utan konserveringsmedel	Prednisolone (as prednisolone sodium phosphate) 100 microgram/mL eye solution
prednisolon 0,03 %, ögondroppar	Product containing precisely prednisolone (as prednisolone sodium phosphate) 300 microgram/1 milliliter conventional release eye solution (clinical drug)
prednisolon 0,03 %, ögondroppar	Product containing precisely prednisolone (as prednisolone sodium phosphate) 300 microgram/1 milliliter conventional release eye solution (clinical drug)
prednisolon 0,03 %, ögondroppar utan konserveringsmedel	Product containing precisely prednisolone (as prednisolone sodium phosphate) 300 microgram/1 milliliter conventional release eye solution (clinical drug)
prednisolon 0,1 %, ögondroppar	Prednisolone (as prednisolone sodium phosphate) 1 mg/mL eye solution
prednisolon 0,1 %, ögondroppar	Prednisolone (as prednisolone sodium phosphate) 1 mg/mL eye solution
prednisolon 0,1 %, ögondroppar utan konserveringsmedel	Prednisolone (as prednisolone sodium phosphate) 1 mg/mL eye solution
prednisolon 0,3 %, ögondroppar	Product containing precisely prednisolone (as prednisolone sodium phosphate) 300 microgram/1 milliliter conventional release eye solution (clinical drug)
prednisolon 0,3 %, ögondroppar	Product containing precisely prednisolone (as prednisolone sodium phosphate) 3 milligram/1 milliliter conventional release eye solution (clinical drug)
prednisolon 0,3 %, ögondroppar utan konserveringsmedel	Product containing precisely prednisolone (as prednisolone sodium phosphate) 300 microgram/1 milliliter conventional release eye solution (clinical drug)
Prednisolone 20mg/100mL enema	Prednisolone only product in rectal dose form
Prednisolone 20mg/100mL enema	Prednisolone only product in rectal dose form
prednisolon 20 mg/100 ml, retentionslavemang som administreras med lång slang	Prednisolone only product in rectal dose form
prednisolon 20 mg/100 ml, retentionslavemang som administreras med standardslang	Prednisolone only product in rectal dose form
prednisolon 5 mg, löslig tablett	Product containing precisely prednisolone 5 milligram/1 each conventional release orodispersible tablet (clinical drug)
prednisolonacetat 5 mg + natriumsulfacetamid 100 mg, salva	Prednisolone and sulfacetamide only product in ocular dose form
Prednisolone acetate 25mg/mL	Product containing precisely prednisolone 25 milligram/1 milliliter conventional release eye suspension (clinical drug)
prednisolonacetat 25 mg/ml, suspension	Product containing precisely prednisolone 25 milligram/1 milliliter conventional release eye suspension (clinical drug)
allergi mot prednisolondroppar	Allergy to prednisolone
prednisolonhexanoat 1,3 mg + cinkokain 1 mg, suppositorium	Product containing precisely cinchocaine 1 milligram and prednisolone (as prednisolone sodium phosphate) 1.3 milligram/1 each conventional release rectal suppository (clinical drug)
prednisolonnatriumfosfat 0,5 %, ögondroppar	Prednisolone (as prednisolone sodium phosphate) 5 mg/mL eye solution
prednisolonnatriumfosfat 0,5 %, ögondroppar för engångsbruk	Prednisolone (as prednisolone sodium phosphate) 5 mg/mL eye solution
prednisolonnatriumfosfat 1 %, lösning	Product containing precisely prednisolone sodium phosphate 10 milligram/1 milliliter conventional release eye drops (clinical drug)
prednisolonnatriumfosfat 1/8 %, lösning	Product containing precisely prednisolone 1.25 milligram/1 milliliter conventional release eye solution (clinical drug)
preferens för temperatur på dryck	Preference for temperature of drink (observable entity)
preferens för temperatur på mat	Preference for temperature of food (observable entity)
Preglaucoma	Glaucoma suspect
substansberoende under graviditet	Pregnancy and substance dependence (disorder)
förlängd graviditet-41 veckor	Prolonged pregnancy (disorder)
förlängd graviditet-42 veckor	Prolonged pregnancy (disorder)
Pregnancy, childbirth and puerperal disorders	Disorder of pregnancy
prematur onormal placenta	Premature aging of placenta
Premature ejaculation	Premature ejaculation
underburet foster	Prematurity of infant (disorder)

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001156010	REPLACED BY 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)
900000000001157018	REPLACED BY association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)