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 - delivered with postnatal complication	A maternal disorder that occurs within the puerperium whose natural progress is impacted or complicated directly or indirectly by the associated disorder and/or the disorder is predisposed to by the physiological circumstances of the postpartum.
Complications of the puerperium NOS with postnatal complication	A maternal disorder that occurs within the puerperium whose natural progress is impacted or complicated directly or indirectly by the associated disorder and/or the disorder is predisposed to by the physiological circumstances of the postpartum.
Complications of the puerperium NOS, unspecified	A maternal disorder that occurs within the puerperium whose natural progress is impacted or complicated directly or indirectly by the associated disorder and/or the disorder is predisposed to by the physiological circumstances of the postpartum.
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
Component of Apgar score	Neonate observable
Compound antacids	Antacid (substance)
Compound anti-infective preparations	Anti-infective agent (substance)
Compound antispasmodics	Antispasmodic (substance)
Compound bronchodilators	Bronchodilator (substance)
Compressed air	Compressed air
Compression NOS	Compression bandaging
Compression NOS	Compression bandaging
Compression of spinal nerve root, NEC	Compression of spinal nerve root
Compulsive neurosis	Obsessive-compulsive disorder
Compulsive overt homosexual state	Hypersexuality state
Computed tomography discogram	CT discogram with injection of contrast into intervertebral disc
Computed tomography discogram of cervical region	CT discogram with injection of contrast into intervertebral disc of cervical spine
Computed tomography discogram of lumbar region	CT discography with injection of contrast into intervertebral disc of lumbar spine
Computed tomography discogram of thoracic 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	Fetal disorder originating in perinatal period (disorder)
Condition of umbilical cord at delivery	Umbilical cord feature
Conduct of delivery NOS	Delivery procedure (procedure)
Conduct of delivery NOS	Delivery procedure (procedure)
Conduction disorders NOS	Any abnormal alteration of atrioventricular conduction.
Conduction disorders NOS	Any abnormal alteration of atrioventricular conduction.
Cone biopsy of cervix uteri NEC	Cone biopsy of cervix
Cone biopsy of cervix uteri NEC	Cone biopsy of cervix
Cone cells of inner nuclear layer	Cone of retina
Cone monochromatism	Blue cone monochromatism (disorder)
Confidential data NOS	Confidential patient data held (finding)
Confidential data NOS	Confidential patient data held (finding)
Congener toxicity	Polychlorinated biphenyl poisoning
Congenital CNS anomalies NOS	Congenital anomaly of central nervous system
Congenital CNS anomalies NOS	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
Congenital CVS anomaly NOS	Congenital anomaly of cardiovascular system
Congenital abnormal fusion	Fusion that has occurred in a structure that is not normally fused.
Congenital abnormal number	Abnormal number (morphologic abnormality)
Congenital abnormality of uterus affecting obstetric care	Congenital abnormality of uterus in pregnancy, childbirth and the puerperium
Congenital anomaly NOS	Congenital malformation
Congenital anomaly NOS	Congenital malformation
Congenital anomaly NOS	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
Congenital atresia	Atresia (morphologic abnormality)
Congenital atresia of pulmonary valve NOS	Congenital atresia of pulmonary valve
Congenital cataract	Abnormally opaque structure (morphologic abnormality)
Congenital cerebral cyst NOS	Congenital cyst of brain (disorder)
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 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 cystic dilatation with accumulation of fluid	Cystic dilatation with accumulation of fluid
Congenital deformity	Deformity
Congenital dislocation of hip NOS	Congenital dislocation of hip
Congenital dislocation of hip NOS	Congenital dislocation of hip
Congenital dystrophia brevicollis	Klippel-Feil sequence
Congenital dystrophia brevicollis	Klippel-Feil sequence
Congenital endaural hernia	Encephalocele
Congenital giant pigmented nevus of skin	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.
Congenital hereditary endothelial dystrophy type 1	Polymorphous corneal dystrophy
Congenital imperforation, high	Atresia (morphologic abnormality)
Congenital imperforation, low	Atresia (morphologic abnormality)
Congenital incomplete expansion of lung	Perinatal atelectasis
Congenital leukocyte adherence deficiency	Leukocyte adhesion deficiency
Congenital lordosis	Congenital lordosis deformity of spine (disorder)
Congenital macrocolon, not aganglionic	Congenital dilatation of colon
Congenital malformation syndromes affecting facial appearance	Multiple malformation syndrome with facial defects as major feature
Congenital malformation syndromes involving limbs	Multiple malformation syndrome with limb defect as major feature
Congenital malposition, left	Left malposition (morphologic abnormality)
Congenital malposition, right	Right malposition (morphologic abnormality)
Congenital medial deviation	Medial displacement
Congenital misalignment	Misalignment (morphologic abnormality)
Congenital musculoskeletal anomalies NOS	Congenital anomaly of musculoskeletal system
Congenital musculoskeletal anomalies NOS	Congenital anomaly of musculoskeletal system
Congenital myelin deficiency of the optic disc	Congenital anomaly of optic disc
Congenital night blindness NOS	Congenital stationary night blindness
Congenital pancreatic enterokinase deficiency	Intestinal enteropeptidase deficiency
Congenital postural lordosis	Congenital lordosis deformity of spine (disorder)
Congenital premature fusion	Premature fusion
Congenital pseudoarthrosis	Pseudoarthrosis
Congenital ridge ear	Congenital deformity of pinna
Congenital sequestration	Sequestration (morphologic abnormality)
Congenital smallness	Abnormal smallness (morphologic abnormality)
Congenital thrombocytopenic purpura	Upshaw-Schulman syndrome (disorder)
Congenital trigger thumb	Pediatric trigger thumb
Congenital trigger thumb of bilateral hands	Pediatric locking of interphalangeal joint of bilateral thumbs (disorder)
Congenital trigger thumb of left hand	Pediatric trigger thumb of left hand
Congenital trigger thumb of right hand	Pediatric locking of interphalangeal joint of right thumb (disorder)
Congenital von Willebrand's disease	A rare, inherited bleeding disorder characterized by defective platelet adhesion and secondary coagulation defect that manifests as abnormal bleeding of variable severity occurring either spontaneously or in association with an invasive procedure. Three main subtypes are defined based on the type of von Willebrand factor defect: partial (type 1) or total (type 3) deficiency, and qualitative/functional anomalies (type 2).
Congenital von Willebrand's disease type I	A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF).
Congenital von Willebrand's disease type II	A form of von Willebrand disease (VWD) characterised by a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (VWF). Depending on the type of functional abnormalities, this form is classified as type 2A, 2B, 2M or 2N.

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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)