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
Deficiency of endopeptidase	Deficiency of protease (disorder)
Deficiency of endopeptidase	Deficiency of endopeptidase
Deficiency of factor II &/or prothrombin	Factor II deficiency
Deficiency of gluconolactonase	Deficiency of gluconolactonase
Deficiency of gluconolactonase	Deficiency of aldonolactonase
Deficiency of gluconolactonase	Deficiency of lactonase
Deficiency of glycosidase	Deficiency of amylase
Deficiency of glycosidase	Deficiency of glycosidase
Deficiency of inosine nucleosidase	Deficiency of inosinase
Deficiency of inosine nucleosidase	Deficiency of inosine nucleosidase
Deficiency of oligo-1,6-glucosidase	Deficiency of isomaltase
Deficiency of oligo-1,6-glucosidase	Sucrase-isomaltase deficiency
Deficiency of palmitoyl-CoA hydrolase	Deficiency of palmitoyl-CoA hydrolase
Deficiency of palmitoyl-CoA hydrolase	Deficiency of long-chain fatty-acyl-CoA hydrolase
Deficiency of pectinesterase	Deficiency of pectin methylesterase
Deficiency of pectinesterase	Deficiency of pectinesterase
Deficiency of pectinesterase	Deficiency of pectin methoxylase
Deficiency of phospholipase D	Deficiency of lecithinase D
Deficiency of phospholipase D	Deficiency of lipophosphodiesterase II
Deficiency of phospholipase D	Deficiency of phospholipase D
Deficiency of phosphoric monoester hydrolase	Deficiency of phosphatase
Deficiency of phosphoric monoester hydrolase	Deficiency of phosphoric monoester hydrolase
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 phosphorylase b kinase
Deficiency of protein kinase	Deficiency of hydroxyalkyl-protein kinase (disorder)
Deficiency of sulfuric ester hydrolase	Deficiency of sulfatase
Deficiency of sulfuric ester hydrolase	Deficiency of sulphuric ester hydrolase
Deficiency of trypsin	Deficiency of alpha- and beta-trypsin
Deficiency of trypsin	Deficiency of trypsin
Deficiency of vitamin A (disorder)	Disorder of vitamin A
Deficiency of vitamin A (disorder)	Vitamin A deficiency
Deficiency of vitamin B>12< (disorder)	Disorder of vitamin B12 (disorder)
Deficiency of vitamin B>12< (disorder)	Cobalamin deficiency
Deficiency of vitamin D (disorder)	Vitamin D deficiency
Deficiency of vitamin D (disorder)	Disorder of vitamin D (disorder)
Deficiency of vitamin D>2< (disorder)	Disorder of vitamin D2 (disorder)
Deficiency of vitamin D>2< (disorder)	Deficiency 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
Deficiency of vitamin K>1< (disorder)	Disorder of vitamin K1 (disorder)
Deficiency of vitamin K>1< (disorder)	Deficiency of vitamin K1 (disorder)
Deficiency of vitamin K>2< (disorder)	Deficiency of vitamin K2 (disorder)
Deficiency of vitamin K>2< (disorder)	Disorder of vitamin K2 (disorder)
utilstrækkelig viden	Healthcare knowledge finding (finding)
Deformation of breast	Deformity of breast
Deformation of breast	Deformation of breast
Deformity of calcaneum (& acquired)	Deformity of calcaneum
Deformity of carpal bone	Deformity of carpal bone
Deformity of clavicle	Acquired deformity of clavicle
Deformity of femur (& acquired)	Deformity of femur
Deformity of fibula	Deformity of fibula
Deformity of humerus (& acquired)	Deformity of humerus
deformitet af ben	Deformity of lower leg
deformitet af ben	Deformity of lower limb (finding)
Deformity of metacarpal (& acquired)	Deformity of metacarpal
Deformity of metatarsal	Deformity of metatarsal
Deformity of patella	Deformity of patella
Deformity of pelvis (& acquired)	Acquired deformity of bone of pelvis
Deformity of pelvis (& acquired)	Acquired deformity of pelvic region (disorder)
Deformity of pelvis (& acquired)	Deformity of bone of pelvis (disorder)
Deformity of pelvis (& acquired)	Deformity of pelvic region (disorder)
deformitet af pelvis	Deformity of pelvic region (disorder)
deformitet af pelvis	Deformity of bone of pelvis (disorder)
Deformity of phalanx of finger or thumb	Deformity of phalanx of finger or thumb
Deformity of phalanx of toe (& acquired)	Deformity of phalanx of toe
Deformity of radius	Deformity of radius
Deformity of scapula (& acquired)	Acquired deformity of scapula
Deformity of scapula (& acquired)	Deformity of scapula (disorder)
Deformity of scapula (& acquired)	Congenital anomaly of scapula
Deformity of talus	Deformity of talus
Deformity of tibia (& acquired)	Deformity of tibia
Deformity of ulna (& acquired)	Deformity of ulna
Deformity/haematoma of pinna	Deformity of pinna
Deformity/haematoma of pinna	Hematoma of pinna
deformitet/hæmatom i auricula	Hematoma of pinna
deformitet/hæmatom i auricula	Deformity of pinna
Degenerated globe condition NOS	Degenerative disorder of eye
Degenerating leiomyoma	Hydropic leiomyoma (morphologic abnormality)
Degenerating leiomyoma	Degenerative abnormality
Degenerating leiomyoma	Leiomyoma
Degeneration af cervikotorakal intervertebral discus	Degeneration of thoracic intervertebral disc
Degeneration af cervikotorakal intervertebral discus	Degeneration of seventh cervical intervertebral disc (disorder)
Degeneration af cervikotorakal intervertebral discus	Degeneration of cervical intervertebral disc
Degeneration af macula og bageste linsepol	Degeneration of posterior pole of eye
Degeneration af macula og bageste linsepol	Degenerative disorder of macula (disorder)
Degeneration of macula or posterior pole NOS	Degeneration of posterior pole of eye
Degeneration of macula or posterior pole NOS	Degenerative disorder of macula (disorder)
Degeneration of macular due to cyst &/or hole &/or pseudohole	Macular hole
Degeneration of macular due to cyst &/or hole &/or pseudohole	Degeneration of macula due to cyst, hole or pseudohole
Degenerativ OG/ELLER vaskulær sygdom i øret	Disorder of blood vessel (disorder)
Degenerativ OG/ELLER vaskulær sygdom i øret	Degenerative disorder of ear (disorder)
degenerative og vaskulære forstyrrelser i øre	Degenerative disorder of ear (disorder)
degenerative og vaskulære forstyrrelser i øre	Disorder of blood vessel (disorder)
Degenerative and vascular disorders of ear NOS	Degenerative disorder of ear (disorder)
Degenerative and vascular disorders of ear NOS	Disorder of blood vessel (disorder)
Degenerative arthropathy	Rheumatoid arthritis
Degenerative arthropathy	Osteoarthritis (disorder)
Degenerativ artropati af spinalt facetled	Osteoarthritis of spinal facet joint

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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)