900000000000531004: referentieset voor associaties betreffende verplaatste beschrijvingen (metadata)

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

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:

Expanded Value Set

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

Members	targetComponentId
Congenital absence of oviduct	Congenital absence of oviduct (disorder)
Congenital absence of testis, unilateral	Congenital absence of testis (disorder)
Congenital afibrinogenaemia	Congenital afibrinogenaemia
Congenital afibrinogenemia	Congenital afibrinogenaemia
Congenital anomaly of umbilical artery	Congenital anomaly of umbilical artery (disorder)
Congenital cardiovascular disorder	Congenital cardiovascular disorder (disorder)
Congenital common duct cyst	Congenital cystic dilatation of common bile duct
Congenital coronary arteriovenous fistula	Congenital coronary arteriovenous fistula
Congenital crooked finger	Congenital clinodactyly of finger
Congenital cystic dilatation of common bile duct	Congenital choledochal cyst (disorder)
Congenital deformity of lower limb	Congenital deformity of lower limb (disorder)
Congenital deformity of musculoskeletal system	Congenital deformity of musculoskeletal system (disorder)
Congenital deformity of scapula	Congenital deformity of scapula (disorder)
Congenital discoid lateral meniscus	Congenital discoid lateral meniscus of knee (disorder)
Congenital endocardial fibroelastosis	Congenital endocardial fibroelastosis (disorder)
Congenital folate malabsorption	Congenital folate malabsorption anaemia
Congenital generalised fibromatosis	Congenital generalized fibromatosis (morphologic abnormality)
Congenital generalised fibromatosis	Infantile myofibromatosis
Congenital generalized fibromatosis	Infantile myofibromatosis
Congenital generalized fibromatosis	Congenital generalized fibromatosis (morphologic abnormality)
Congenital giant pigmented naevus	Pigmented nevus
Congenital giant pigmented nevus	Pigmented nevus
Congenital glottic web of larynx	Congenital glottic web of larynx (disorder)
Congenital hydrocele of canal of Nuck	Congenital hydrocele of canal of Nuck (disorder)
Congenital hypofibrinogenaemia	Congenital hypofibrinogenemia (disorder)
Congenital hypofibrinogenemia	Congenital hypofibrinogenemia (disorder)
Congenital hypothyroidism	Congenital hypothyroidism
Congenital ichthyosis	Congenital ichthyosis of skin
Congenital iodine deficiency hypothyroidism	Congenital iodine deficiency syndrome
Congenital iodine deficiency syndrome	Congenital iodine deficiency syndrome
Congenital iodine deficiency syndrome - myxedematous type	Endemic congenital iodine deficiency syndrome of myxedematous type (disorder)
Congenital iodine deficiency syndrome - myxoedematous type	Endemic congenital iodine deficiency syndrome of myxedematous type (disorder)
Congenital lordosis due to bony malformation	Congenital lordosis deformity of spine due to congenital malformation of skeletal bone (disorder)
Congenital malformation due to valproic acid	Congenital malformation caused by valproic acid
Congenital malformation of inner ear	Congenital anomaly of inner ear
Congenital malformation of lens	Congenital anomaly of lens (disorder)
Congenital megacalycosis	Congenital megacalycosis (disorder)
Congenital monosaccharide malabsorption	Congenital monosaccharide malabsorption
Congenital multiple arthrogryposis	Arthrogryposis multiplex congenita
Congenital multiple arthrogryposis	Arthrogryposis multiplex congenita
Congenital narrowed pulmonary artery	Congenital stenosis of pulmonary artery (disorder)
Congenital paraplegia	Congenital paraplegia
Congenital rectal stenosis	Congenital rectal stenosis
Congenital rhabdomyomatous mesenchymal hamartoma	Congenital rhabdomyomatous mesenchymal hamartoma
Congenital sensorineural deafness	Congenital sensorineural hearing loss (disorder)
Congenital skin contracture	Congenital skin contracture
Congenital spasm of pylorus	Congenital pyloric spasm
Congenital stenosis of pulmonary artery	Congenital stenosis of pulmonary artery (disorder)
Congenital stenosis of pylorus	Congenital pyloric stenosis
Congenital stricture of anus	Congenital stricture of anus
Congenital stricture of pulmonary artery	Congenital stenosis of pulmonary artery (disorder)
Congenital subglottic web of larynx	Congenital subglottic web of larynx
Congenital ulnar negative variant of wrist	Congenital negative ulnar variant of wrist (disorder)
Congenital ulnar negative variant wrist	Congenital negative ulnar variant of wrist (disorder)
Congenital umbilical granuloma	Umbilical granuloma
Conical tooth	Peg-shaped tooth (disorder)
Constant observation	Constant observation (regime/therapy)
Constant watching	Constant observation (regime/therapy)
Construction of cutaneous ureteroileostomy	Construction of cutaneous ureteroileostomy
Construction of diverting colostomy	Loop colostomy (procedure)
Construction of pouch	Construction of pouch
Consultation for radiotherapy	Consultation for radiotherapy (procedure)
Continuous curvilinear capsulorhexis	Capsulorrhexis of lens capsule (procedure)
Continuous curvilinear capsulorrhexis	Capsulorrhexis of lens capsule (procedure)
Contraception counseling	Contraceptive counseling
Contraception counselling	Contraceptive counseling
Contraceptive cap	Vaginal contraceptive cap
Contrast media allergy	Allergy to contrast media
Convalescent plasma transfusion therapy	Therapeutic transfusion of convalescent plasma (procedure)
Conventional central osteosarcoma	Conventional central osteosarcoma (morphologic abnormality)
Cordylobia	Genus Cordylobia (organism)
Coronary artery disease excluded	Coronary artery disease absent (situation)
Coronary artery fistula	Coronary artery fistula (disorder)
Corpus fibrosum of ovary	Structure of corpus fibrosum of ovary
Correction of bat ear	Repair of bat ear (procedure)
Correction of congenital choanal atresia	Repair of choanal atresia (procedure)
Correction of congenital choanal stenosis	Repair of choanal atresia (procedure)
Correction of congenital talipes equinovarus	Correction of congenital talipes equinovarus (procedure)
Corticospinal tract	Structure of corticospinal tract (body structure)
Corticotroph adenoma	Corticotroph pituitary adenoma (morphologic abnormality)
Cow milk specific IgE antibody measurement	Cow's milk specific immunoglobulin E antibody measurement (procedure)
Cranial puncture	Cranial puncture
Cranial root of accessory nerve	Cranial root of accessory nerve
Cranial tap	Cranial puncture
Creation of conjunctival flap	Creation of conjunctival flap
Creation of gastrostomy	Gastrostomy
Crohn's regional enteritis	Crohn's disease of small intestine
Cross-dressing	Cross-dressing
Crystal	Crystal
Crystal	Crystal
Crystals	Crystal
Crystals	Crystal
Cubital tunnel	Structure of cubital tunnel (body structure)
Cup	Cup
Curling's ulcer of stomach	Curling's ulcers
Curvularia spicifera	Bipolaris spicifera
Cutaneous route	Cutaneous route (qualifier value)
Cutaneous use	Cutaneous route (qualifier value)
Cyanosis	Cyanosis
Cylindrical cell papilloma	Oncocytic Schneiderian papilloma of uncertain behavior (morphologic abnormality)
Cylindrocarcinoma	Malignant neoplasm arising from pre-existing cylindroma

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
900000000001166019	REFERS TO concept association reference set	en	Synonym (core metadata concept)	Active	Entire term case sensitive (core metadata concept)	SNOMED CT model component module (core metadata concept)
900000000001167011	REFERS TO concept 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)
9038881000146119	referentieset voor associaties betreffende verplaatste beschrijvingen	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
14125871000146116	referentieset voor associaties betreffende verplaatste beschrijvingen (metadata)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)