1186921001: POSSIBLY 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)\POSSIBLY REPLACED BY association reference set (foundation metadata concept)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Nov 2021. Module: SNOMED CT model component module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module

4668053013 POSSIBLY 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)

4668054019 POSSIBLY 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
POSSIBLY REPLACED BY association reference set (foundation metadata concept)	Is a	Historical association reference set (foundation metadata concept)	true	Inferred relationship	Some

Members	targetComponentId
Conventional release suspension for infusion and/or injection	Suspension for injection
Conventional release suspension for infusion and/or injection	Dispersion for infusion
Diagnostic pneumomediastinum	Plain X-ray of chest (procedure)
Diagnostic pneumomediastinum	CT of mediastinum
Diagnostic pneumomediastinum	Computed tomography of mediastinum with contrast (procedure)
Diagnostic pneumomediastinum	Magnetic resonance imaging of mediastinum (procedure)
Disability assessment schedule	WHODAS (World Health Organization Disability Assessment Schedule) 2.0 12-item short version
Disability assessment schedule	World Health Organization Disability Assessment Schedule 2.0 36-item full version (assessment scale)
Disorder due to alcohol abuse	Disorder caused by alcohol (disorder)
Disorder due to alcohol abuse	Disorder characterized by the pattern and consequences of alcohol use leading to clinically significant impairment or distress both to physical or mental health of the user or others around the user.
Drug habituation	The inability to regulate the use of a specified substance due to repeated or continuous use. Key features include a strong internal drive to use the substance, impaired control over use, prioritizing use over other activities, and continued use despite harm or negative consequences. This often comes with urges or cravings. Physiological dependence may also occur, marked by tolerance, withdrawal symptoms, or use of the substance to prevent withdrawal. These features typically appear over 12 months but can be diagnosed if use is continuous for at least 3 months.
Drug habituation	A range of disorders stemming from the single or repeated use of predominantly psychoactive substances, including certain medications. Initially, these substances provide pleasurable effects, encouraging further use. Over time, however, this can lead to dependence and severe mental and physical health issues. These disorders also cover harmful non-medical use of non-psychoactive substances. They result in significant impairment, exhibiting cognitive, behavioural, and physiological symptoms, and persist despite adverse consequences, underscoring their complex and damaging impact.
Duodenum double contrast exam.	CT of duodenum
Duodenum double contrast exam.	Computed tomography of duodenum with contrast (procedure)
Duodenum double contrast exam.	Magnetic resonance imaging of duodenum (procedure)
Duodenum double contrast exam.	Fluoroscopic duodenography (procedure)
Duodenum double contrast examination	Computed tomography of duodenum with contrast (procedure)
Duodenum double contrast examination	CT of duodenum
Duodenum double contrast examination	Magnetic resonance imaging of duodenum (procedure)
Duodenum double contrast examination	Fluoroscopic duodenography (procedure)
Dupuytren's contracture	Focal fibromatosis
Dupuytren's contracture	Contracture
Dupuytren's contracture	Fibrous bands
Early onset generalized periodontitis	Periodontitis as manifestation of systemic disease (disorder)
Early onset generalized periodontitis	Aggressive periodontitis
Early onset localized periodontitis	Aggressive periodontitis
Early onset localized periodontitis	Periodontitis as manifestation of systemic disease (disorder)
Early onset periodontitis	Aggressive periodontitis
Early onset periodontitis	Periodontitis as manifestation of systemic disease (disorder)
Echogynography	US gynaecology scan
Echogynography	Ultrasound procedure on female genital system AND/OR pregnancy related structure (procedure)
Ehlers-Danlos syndrome, non hydroxylysine deficient ocular type	A rare systemic disease characterized by congenital multiple contractures, characteristic craniofacial features (like large fontanel, hypertelorism, downslanting palpebral fissures, blue sclerae, ear deformities, high palate) evident at birth or in early infancy, and characteristic cutaneous features like skin hyperextensibility, skin fragility with atrophic scars, easy bruising, and increased palmar wrinkling. Additional features include recurrent/chronic dislocations, chest and spinal deformities, peculiarly shaped fingers, colonic diverticula, pneumothorax, and urogenital and ophthalmological abnormalities, among others. Molecular testing is obligatory to confirm the diagnosis.
Ehlers-Danlos syndrome, non hydroxylysine deficient ocular type	A rare, hereditary connective tissue disease characterized by severe ocular manifestations due to extreme corneal thinning and fragility with rupture in the absence of significant trauma, often leading to irreversible blindness. Extraocular manifestations comprise deafness, developmental hip dysplasia, and joint hypermobility.
Endotracheal bronchography	Fluoroscopy of bronchus with contrast
Endotracheal bronchography	Computed tomography of bronchus with contrast (procedure)
Entire middle cells of ethmoid sinus	Entire anterior cells of ethmoid sinus
Entire middle cells of ethmoid sinus	Entire posterior cells of ethmoid sinus
Entire posterior, lateral and septal nasal arteries	Entire dorsal nasal artery
Entire posterior, lateral and septal nasal arteries	Entire lateral nasal artery (body structure)
Epilepsy characterized by intractable complex partial seizures	Drug resistance to anti-seizure medication (disorder)
Epilepsy characterized by intractable complex partial seizures	A type of epilepsy with only focal onset epileptic seizures. Seizures can arise from a single location or multiple locations.
Family history of handicap	Family history of intellectual disability
Family history of handicap	Family history of disability
Family history of handicap	Family history of learning disability
Fetography	Magnetic resonance imaging of fetus (procedure)
Fetography	Ultrasonography for antepartum monitoring of fetus
Fetus or neonate affected by ectopic pregnancy NOS	Ectopic pregnancy
Fetus or neonate affected by ectopic pregnancy NOS	Combined pregnancy
Fetus or neonate affected by unspecified ectopic pregnancy	Combined pregnancy
Fetus or neonate affected by unspecified ectopic pregnancy	Ectopic pregnancy
Fusion by stapling	A closure done by stapling
Fusion by stapling	Procedure to cause two adjacent structures to be structurally joined together
Generalized non-convulsive absence epilepsy	A type of epilepsy that presents with daily typical absence seizures usually between 4 to 10 years of age in an otherwise normal child. Absence seizures are brief but may occur in clusters and are provoked by hyperventilation. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram shows 2.5 to 4 Hz generalized spike-wave and a normal background.
Generalized non-convulsive absence epilepsy	A type of epilepsy that presents with typical absence seizures between 9 and 13 years of age in an otherwise normal adolescent. The typical absence seizures usually occur less than daily in the untreated state and are provoked by hyperventilation in 87 percent of cases. Generalized tonic-clonic seizures are seen in greater than 90 percent of cases, most commonly beginning shortly after onset of absence seizures. Myoclonic seizures do not occur. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram shows 3 to 5.5 Hz generalized spike-wave with a normal background.
Generalized non-convulsive absence epilepsy	A type of epilepsy with only generalised onset epileptic seizures.
Goodal-Power operation on vagina	Colpocleisis, Le Fort type
Goodal-Power operation on vagina	Operation on vagina
Gynecogram	CT of female genital tract
Gynecogram	MRI of female genital tract
Gynecogram	CT of female genital tract with contrast
Gynecogram	MRI of female genital tract with contrast
Gynecogram	Fluoroscopy of female genital tract with contrast (procedure)
Handicapped aids (& for severely handicapped)	Provision of aid for severe disability
Handicapped aids (& for severely handicapped)	Provision of aid for disability (procedure)
Handicapped: [relative - physically] or [spouse] or [child]	Child of subject has disability (situation)
Handicapped: [relative - physically] or [spouse] or [child]	Spouse has disability (situation)
Handicapped: [relative - physically] or [spouse] or [child]	Family history of disability
Hepaticostomy with removal of calculus	Hepaticostomy
Hepaticostomy with removal of calculus	Removal of calculus from liver
Hepaticotomy with removal of calculus	Removal of calculus from liver
Hepaticotomy with removal of calculus	Hepaticostomy
Husband alcoholic	Husband has alcohol dependence
Husband alcoholic	Husband has alcohol use disorder (situation)
Hysterical fever	Pyrexia of unknown origin
Hysterical fever	Factitious fever
Hysterical macropsia	Macropsia (disorder)
Hysterical macropsia	Dissociative neurological symptom disorder with visual symptom (disorder)
Hysterical micropsia	Micropsia (disorder)
Hysterical micropsia	Dissociative neurological symptom disorder with visual symptom (disorder)
Infantile spasms co-occurrent with status epilepticus	An abnormally prolonged continuous epileptic seizure or cluster of epileptic seizures in which the individual does not return to normal between seizures. The definition of abnormal duration varies based on seizure type.
Infantile spasms co-occurrent with status epilepticus	Epileptic spasms are a sudden flexion, extension, or mixed extension-flexion of predominantly proximal and truncal muscles, regardless of whether focal, generalised, or unknown onset, and whether aware or impaired awareness. An epileptic spasm is usually more sustained than a myoclonic movement but not as sustained as a tonic seizure. Limited forms may occur including grimacing, head nodding, or subtle eye movements. Epileptic spasms frequently occur in clusters.
Intracavitary brachytherapy of female genital tract	Insertion of uterine cesium applicators
Intracavitary brachytherapy of female genital tract	Insertion of vaginal caesium applicators
Intractable idiopathic partial epilepsy	A type of epilepsy with only focal onset epileptic seizures. Seizures can arise from a single location or multiple locations.
Intractable idiopathic partial epilepsy	Drug resistance to anti-seizure medication (disorder)
Intractable partial frontal lobe epilepsy with impairment of consciousness	Drug resistance to anti-seizure medication (disorder)
Intractable partial frontal lobe epilepsy with impairment of consciousness	A type of focal epilepsy where all the seizures originate within the frontal lobe.
Intractable partial occipital lobe epilepsy with impairment of consciousness	Occipital lobe epilepsy
Intractable partial occipital lobe epilepsy with impairment of consciousness	Drug resistance to anti-seizure medication (disorder)
Intractable partial parietal lobe epilepsy with impairment of consciousness	Drug resistance to anti-seizure medication (disorder)
Intractable partial parietal lobe epilepsy with impairment of consciousness	A type of focal epilepsy where all the seizures originate within the parietal lobe.
Intractable partial temporal lobe epilepsy with impairment of consciousness	A type of focal epilepsy where all the seizures originate within the temporal lobe.
Intractable partial temporal lobe epilepsy with impairment of consciousness	Drug resistance to anti-seizure medication (disorder)
Intractable simple partial epilepsy	A type of epilepsy with only focal onset epileptic seizures. Seizures can arise from a single location or multiple locations.
Intractable simple partial epilepsy	Drug resistance to anti-seizure medication (disorder)
Intravenous cholangiogram	Fluoroscopic T tube cholangiography with contrast
Intravenous cholangiogram	Fluoroscopic cholangiography with contrast (procedure)
Intravenous cholangiogram	Computed tomography cholangiography with contrast (procedure)
Intravenous cholangiography	Fluoroscopic T tube cholangiography with contrast
Intravenous cholangiography	Computed tomography cholangiography with contrast (procedure)
Intravenous cholangiography	Fluoroscopic cholangiography with contrast (procedure)

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Reference Sets

Reference set descriptor

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Id	Description	Lang	Type	Status	Case?	Module
4668053013	POSSIBLY 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)
4668054019	POSSIBLY 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)