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
Common peroneal nerve disorder-retired	Common peroneal nerve paralysis (disorder)
Common peroneal nerve disorder-retired	Common peroneal nerve lesion (disorder)
Common peroneal nerve disorder-retired	Common peroneal neuropathy (disorder)
Common peroneal neuropathy	Common peroneal nerve lesion (disorder)
Common peroneal neuropathy	Common peroneal neuropathy (disorder)
Common peroneal neuropathy	Common peroneal nerve paralysis (disorder)
Common pigweed pollen allergen	Common pigweed pollen
Common reed pollen allergen	Common reed pollen
Common sandgrouse	Pterocles exustus (organism)
Common sorrel pollen allergen	Common sorrel pollen
Common swift	Apus apus (organism)
Communicable disease	Communicable disease
Communicable disease	Contagious disease
Communicable disease, NOS	Communicable disease
Communicating	Communication is a function that endows a person with the capacity to produce, encode, transmit, receive, decode, and interpret information. Communication occurs through a variety of channels, using a variety of signal types. This includes but is not limited to pheromone signals involving chemical channels, body language signals involving musculoskeletal and sensory perceptual channels, written, and spoken language using physiological, mental, and physical/environmental channels. The realisation of this function is the exchange of information between persons, other living organisms, and environments.
Communicating feelings, function	Expression of emotions
Communicating feelings, function	Communicating feelings (observable entity)
Communicating hydrocephalus	Non-obstructive hydrocephalus
Communicating hydrocephalus	Communicating hydrocephalus (disorder)
Communicating hydrocephalus	External hydrocephalus
Community associated methicillin resistant Staphylococcus aureus	Methicillin resistant Staphylococcus aureus
Community based physiotherapy service	Community based physiotherapy service (qualifier value)
Comovirus group	Genus Comovirus (organism)
Comovirus group	Family Comoviridae (organism)
Compensated hypothyroidism	Subclinical hypothyroidism
Compensation for renal failure (& dialysis)	Renal dialysis
Compensation for renal failure (& dialysis)	Haemodialysis
Competitive games psychotherapy	Competitive games psychotherapy (regime/therapy)
Competitive games psychotherapy	Organized games therapy
Complaining of a general symptom NOS	Symptom: generalized
Complaining of cold extremities NOS	Cold extremity
Complaint	Complaint (observable entity)
Complaint	Chief complaint (observable entity)
Complement -third component-C3 (& test)	Complement component C3
Complement 5 dysfunction	Complement 5 dysfunction
Complement 5 dysfunction	Generalized seborrheic dermatitis of infants
Complement C3 fragment measurement	Complement component C3c
Complement C3 fragment measurement	Complement component C3a
Complement C3 fragment measurement	Complement component C3b
Complement C3 fragment measurement	Complement component C3g
Complement C3 fragment measurement	Complement component C3d,g
Complement C3 fragment measurement	Complement component C3d
Complement C3d-C3d+GG-IC3b receptors measurement	CR type 2 receptor measurement
Complement C4 CH50 measurement	C4 complement assay (procedure)
Complement component C4	Lymphocyte antigen CD18
Complement component C4	Complement component C4
Complement factor B	Complement factor B
Complement factor B	Sex steroid binding globulin
Complement haemolytic level	Complement hemolytic assay
Complement-fourth component-C4	Complement component C4
Complete	All members of set
Complete	Total
Complete	Complete
Complete	Completeness
Complete abortion	Complete miscarriage
Complete amputation of penis	Complete amputation of penis
Complete amputation of penis	Radical amputation of penis
Complete breech delivery	Total breech extraction (procedure)
Complete breech delivery	Complete breech delivery
Complete breech delivery	Breech extraction (procedure)
Complete colpocleisis (& Le Fort)	Complete colpocleisis
Complete denture, including adjustments	Fitting of complete denture (procedure)
Complete division, biceps tendon	Traumatic complete division of long head of biceps brachii tendon
Complete division, biceps tendon	Traumatic complete division of both heads of biceps brachii tendon (disorder)
Complete division, both flexor tendons	Complete division flexor tendon hand
Complete division, long head of biceps tendon	Traumatic complete division of long head of biceps brachii tendon
Complete illegal abortion with delayed or excessive hemorrhage	Excessive hemorrhage due to and following induced termination of pregnancy (disorder)
Complete induced termination of pregnancy complicated by delayed or excessive hemorrhage	Excessive hemorrhage due to and following induced termination of pregnancy (disorder)
Complete legal abortion with delayed or excessive hemorrhage	Excessive hemorrhage due to and following induced termination of pregnancy (disorder)
Complete lower denture	Fitting of complete lower denture (procedure)
Complete optic atrophy	Complete optic atrophy
Complete optic atrophy	Atrophy of optic disc
Complete or partial traumatic transection	Complete or partial transection (morphologic abnormality)
Complete or partial traumatic transverse disruption	Acquired crosswise defect in structural continuity of a longitudinal structure.
Complete or partial traumatic transverse rupture	Partial tear (morphologic abnormality)
Complete or partial traumatic transverse rupture	Complete rupture (morphologic abnormality)
Complete overdenture	Fitting of complete overdenture (procedure)
Complete partial seizure of uncertain origin	An epileptic seizure originating within networks limited to one hemisphere. They may be discretely localised or more widely distributed. Focal seizures may originate in subcortical structures.
Complete perineal tear	Fourth degree perineal laceration (disorder)
Complete traumatic transverse rupture	Complete rupture (morphologic abnormality)
Complete trisomy 10 syndrome	Trisomy 10
Complete trisomy 10 syndrome	Mosaic trisomy 10 is a rare chromosomal anomaly syndrome, with a highly variable phenotype, principally characterized by growth delay, craniofacial dysmorphism (including prominent forehead, hypertelorism, upslanting palpebral fissures, blepharophimosis, low-set malformed large ears, high arched palate, cleft lip/palate, retrognathia) and cardiac, renal and skeletal (e.g. radial ray defects, scoliosis) malformations, with death usually occurring neonatally or in early infancy. Other reported features include central nervous system and ear anomalies, as well as facial clefts and anal atresia.
Complete trisomy 14 syndrome	Mosaic trisomy 14 is a rare chromosomal anomaly disorder, with a highly variable phenotype, principally characterized by growth and developmental delay, intellectual disability, body asymmetry/hypotonia, congenital heart defects, genitourinary abnormalities (cryptorchidism, micropenis, large clitoris, labial swelling), and abnormal skin hyperpigmentation. Patients usually present with craniofacial dysmorphism such as microcephaly, abnormal palpebral fissure, hypertelorism, ear abnormalities, broad nose, low-set ears, micro/retro-gnathia, and cleft or highly arched palate.
Complete unilateral cleft palate with cleft lip	Cleft palate with cleft lip
Complete unilateral paralysis	Right hemiplegia
Complete unilateral paralysis	Left hemiplegia
Complete unilateral paresis	Left hemiplegia
Complete unilateral paresis	Right hemiplegia
Complete upper denture	Fitting of complete upper denture (procedure)
Complex V deficiency	Isolated ATP synthase deficiency is a rare, genetic, mitochondrial oxidative phosphorylation disorder that may present with a wide range of symptoms (including muscular hypotonia, hypertrophic cardiomyopathy, psychomotor delay, encephalopathy, peripheral neuropathy, lactic acidosis, 3-methylglutaconic aciduria) and clinical syndromes (including NARP and MILS).
Complex correction by callotasis bone transport	Osteotomy for callotasis prior to correction of bony deformity
Complex correction by callotasis bone transport	Osteotomy for callotasis prior to segmental bone transport
Complex dental caries	Carious exposure of pulp (disorder)
Complex dental caries	Caries involving multiple surfaces of tooth
Complex reconstruction of wrist and hand	Hand reconstruction
Complex reconstruction of wrist and hand	Wrist reconstruction
Complex regional pain syndrome, Type I, of head and/or trunk	Complex regional pain syndrome type I (disorder)
Compliance issues discussed with patient	Encouragement of compliance
Complicated ovarian cyst	Cyst of ovary
Complication affecting body system	Disease
Complication affecting body system	Disorder of body system

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Reference Sets

Reference set descriptor

Description inactivation indicator reference set

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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)