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
Complications of the puerperium NOS	Complication of the puerperium
Komplikationer i puerperium, ikke nærmere specificeret	Complication of the puerperium
Complications of the puerperium NOS	Complication of the puerperium
Complications of the puerperium NOS	Complication of the puerperium
Complications of the puerperium NOS	Complication of the puerperium
komplikationer i puerperium, ikke nærmere specificeret, barn født med postnatal komplikation	Complication of the puerperium
Komplikationer i puerperium, ikke nærmere specificeret med postnatal komplikation	Complication of the puerperium
Komplikationer i puerperium, ikke nærmere specificeret, uspecificeret	Complication of the puerperium
Complications: [surgical and medical care NEC] or [anastomosis (internal)] or [bypass] or [catheter] or [graft] or [implant] or [medical care NEC] or [prosthesis (internal)] or [transplant]	Complication of procedure
Compound antacids	Antacid (substance)
Compound anti-infective preparations	Anti-infective agent (substance)
Compound antispasmodics	Antispasmodic (substance)
Compound bronchodilators	Bronchodilator (substance)
Compound presentation of fetus	Compound presentation
Compressed air	Compressed air (qualifier value)
Kompression, ikke nærmere specificeret	Compression bandaging
Compression NOS	Compression bandaging
Compression of spinal nerve root, NEC	Compression of spinal nerve root
kompulsiv tilstand	Obsessive-compulsive disorder
tvangspræget åbenlys homoseksuel tilstand	Hypersexuality state
CT-diskografi	CT discogram with injection of contrast into intervertebral disc
CT-diskografi af cervikalregionen	CT discogram with injection of contrast into intervertebral disc of cervical spine
CT-diskografi af lumbalregionen	CT discography with injection of contrast into intervertebral disc of lumbar spine
CT-diskografi af torakale region	Computed tomography discography with injection of contrast into intervertebral disc of thoracic spine (procedure)
Computed tomography scan - NOS	Computed tomography (procedure)
Computer record NOS	Computer record status
Computer record NOS	Computer record status
Computerised diagnostic radiology NOS	Computed tomography (procedure)
Computerized diagnostic radiology NOS	Computed tomography (procedure)
Concerned about appearance NOS	Concerned about appearance
Concerned about appearance NOS	Concerned about appearance
Conchal flap	Flap (substance)
Condition in fetus originating in the perinatal period, NEC	Condition in fetus originating in the perinatal period
Navlesnorens tilstand ved forløsning	Umbilical cord feature
Conduct of delivery NOS	Delivery procedure
Conduct of delivery NOS	Delivery procedure
Overledningsforstyrrelser, ikke nærmere specificeret	Any abnormal alteration of atrioventricular conduction.
Conduction disorders NOS	Any abnormal alteration of atrioventricular conduction.
Condyloma latum	Condyloma latum
Cone biopsy of cervix uteri NEC	Cone biopsy of cervix
Keglebiopsi af cervix uteri, ikke klassificeret andetsteds	Cone biopsy of cervix
Cone cells of inner nuclear layer	Cone of retina
Konusmonokromatisme	Blue cone monochromatism (disorder)
Confidential data NOS	Confidential patient data held
Confidential data NOS	Confidential patient data held
congenertoksicitet	Polychlorinated biphenyl poisoning
Congenital CNS anomalies NOS	Congenital anomaly of central nervous system
Kongenitte anomalier i centralnervesystemet, ikke nærmere specificeret	Congenital anomaly of central nervous system
Congenital CNS anomalies NOS	Congenital anomaly of central nervous system
Congenital CVS anomaly NOS	Congenital anomaly of cardiovascular system
Congenital CVS anomaly NOS	Congenital anomaly of cardiovascular system
Kongenit anomali i det kardiovaskulære system, ikke nærmere specificeret	Congenital anomaly of cardiovascular system
kongenit abnorm sammenvoksning	Fusion that has occurred in a structure that is not normally fused.
Kongenit abnormt antal	Abnormal number (morphologic abnormality)
kongenit uterusabnormitet med indvirkning på obstetrisk behandling og pleje	Congenital abnormality of uterus in pregnancy, childbirth and the puerperium
Congenital absence of auricle	Congenital absence of external ear
Congenital absence of eustachian tube	Congenital absence of eustachian tube
Congenital absence of fallopian tube	Congenital atresia of fallopian tube
Congenital anomaly NOS	Congenital malformation
Congenital anomaly NOS	Congenital malformation
kongenit anomali, ikke nærmere specificeret	Congenital malformation
Congenital anomaly NOS	Congenital malformation
Congenital anomaly: [upper GIT NOS] or [oesophagus]	Congenital malformation of upper alimentary tract
Congenital anomaly: [upper GIT NOS] or [oesophagus]	Congenital malformation of upper alimentary tract
kongenit atresi	Atresia (morphologic abnormality)
Kongenit pulmonalklapatresi, ikke nærmere specificeret	Congenital atresia of pulmonary valve
Congenital camptodactyly	Camptodactyly
Congenital cataract	Opacity
kongenit cerebral lammelse, ikke nærmere specificeret	A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain.
Congenital cerebral palsy NOS	A permanent disorder of the development of movement, posture and motor function, causing activity limitation, caused by non-progressive disturbances in the developing fetal or infant brain.
Congenital cyst of kidney	Congenital cystic kidney disease
Congenital cyst of urachus	Allantoic cyst
kongenit cystisk dilatation med væskeakkumulation	Cystic dilatation with accumulation of fluid
Congenital deficiency of pancreatic lipase	Pancreatic triacylglycerol lipase deficiency
kongenit deformitet	Deformity (morphologic abnormality)
kongenit luksation af hofteled, ikke nærmere specificeret	Congenital dislocation of hip
Congenital dislocation of hip NOS	Congenital dislocation of hip
Kongenit endaural hernie	Encephalocele
kongenit pigmenteret kæmpenævus i huden	A rare skin hamartoma characterized by at least one pigmented skin lesion present at birth of more than 20 cm (large congenital melanocytic nevus; LCMN) or 40 cm (giant; GCMN) projected adult diameter. The primary lesion is composed of mutated melanocytes and often locally disorganized epidermal annexes or dermis, and presents with an elevated risk of malignant transformation to melanoma or, more rarely, other neoplasms in skin or central nervous system.
Kongenit hereditær endoteldystrofi type 1	Polymorphous corneal dystrophy
høj kongenit imperforation	Atresia (morphologic abnormality)
lav kongenit imperforation	Atresia (morphologic abnormality)
Congenital incomplete expansion of lung	Perinatal atelectasis
Kongenit leukocytadhæsionsmangel	Leukocyte adhesion deficiency
Congenital lordosis	Congenital lordosis deformity of spine (disorder)
Kongenit megacolon, ikke aganglionær	Congenital dilatation of colon
Kongenitte misdannelsessyndromer, der afficerer ansigtsudseendet	Multiple malformation syndrome with facial defects as major feature
Kongenit misdannelsessyndrom med involvering af ekstremiteter	Multiple malformation syndrome with limb defect as major feature
Kongenit malposition til venstre	Left malposition (morphologic abnormality)
Kongenit malposition til højre	Right malposition (morphologic abnormality)
kongenit medial deviation	Medial displacement
kongenit aksefejl	Misalignment (morphologic abnormality)
Kongenitte muskuloskeletale anomalier, ikke nærmere specificeret	Congenital anomaly of musculoskeletal system
Congenital musculoskeletal anomalies NOS	Congenital anomaly of musculoskeletal system
Kongenit myelinmangel i synsnervepapil	Congenital anomaly of optic disc
Congenital myotonia	Congenital myotonia, autosomal dominant form
Congenital night blindness NOS	Congenital stationary night blindness
Kongenit pankreatisk enterokinasemangel	Intestinal enteropeptidase deficiency
Kongenit postural lordose	Congenital lordosis deformity of spine (disorder)
kongenit præmatur sammenvoksning	Premature fusion
kongenit pseudartrose	Pseudoarthrosis

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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)