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
Pneumography of retroperitoneum	MRI of retroperitoneum
Preload radiotherapy - female genital	Insertion of uterine cesium applicators
Preload radiotherapy - female genital	Insertion of uterine cesium applicators
Preload radiotherapy - female genital	Insertion of vaginal caesium applicators
Preload radiotherapy - female genital	Insertion of vaginal caesium applicators
Prepubertal generalized periodontitis	Periodontitis as manifestation of systemic disease (disorder)
Prepubertal generalized periodontitis	Aggressive periodontitis
Prepubertal periodontitis	Aggressive periodontitis
Prepubertal periodontitis	Periodontitis as manifestation of systemic disease (disorder)
Pressure collapse of lung after anesthesia AND/OR sedation in labor AND/OR delivery	Pressure collapse of lung due to anesthesia during labor and delivery (disorder)
Pressure collapse of lung after anesthesia AND/OR sedation in labor AND/OR delivery	Pressure collapse of lung due to anaesthesia during pregnancy
Pressure collapse of lung after anesthesia AND/OR sedation in labor AND/OR delivery	Pressure collapse of lung due to anesthesia in puerperium
epilessia con assenza generalizzata primaria	Epilepsy with only generalised onset epileptic seizures and generalised spike-wave, due to a genetic or presumed genetic aetiology.
epilessia con assenza generalizzata primaria	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.
epilessia con assenza generalizzata primaria	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.
dysplasie micronodulaire pigmentée des surrénales	Carney complex-associated-primary pigmented nodular adrenocortical disease (disorder)
dysplasie micronodulaire pigmentée des surrénales	A rare adrenocortical nodular disease characterized by increased to normal sized adrenal glands containing multiple small (less than 1 cm in diameter) cortical pigmented (lipofuscin) nodules, surrounded by internodular adrenocortical atrophy. It is typically associated with the development of a form of adrenal Cushing syndrome (CS). Rarely, it has been associated with adrenal macronodules. Whilst PRKAR1A variants are associated with CNC (Carney complex), the mutation c.709-7del6 is mostly associated with i-PPNAD. Other mutations associated with i-PPNAD include PRKACA (germline copy-number gains), PDE11A and PDE8B genes, although these are rare.
Progressive keratoderma tylodes	Chronic irritant contact dermatitis of hands
Progressive keratoderma tylodes	Occupational irritant contact dermatitis (disorder)
Psychologic test, organic battery	Assessment using repeatable battery for the assessment of neuropsychological status (procedure)
Psychologic test, organic battery	Neuropsychological testing
Radiculography	Magnetic resonance imaging of spinal nerve root with contrast (procedure)
Radiculography	MRI of spinal nerve root
mesure radiographique du volume pulmonaire	Lung volume test
mesure radiographique du volume pulmonaire	A pulmonary function test that measures lung volumes
mesure radiographique du volume pulmonaire	A procedure on the respiratory tract that observes pulmonary function
Receptor-positive androgen resistance syndrome	Complete androgen insensitivity syndrome (CAIS) is a form of androgen insensitivity syndrome (AIS), a disorder of sex development (DSD), characterized by the presence of female external genitalia in a 46,XY individual with normal testis development but undescended testes and unresponsiveness to age-appropriate levels of androgens.
Receptor-positive androgen resistance syndrome	A rare difference of sex development (DSD) characterised by the presence of female external genitalia, ambiguous genitalia or variable defects in virilisation in a 46,XY individual with absent or partial responsiveness to age-appropriate levels of androgens. It comprises two clinical subgroups: complete AIS (CAIS) and partial AIS (PAIS).
Receptor-positive androgen resistance syndrome	A difference of sex development (DSD) distinct from complete AIS (CAIS) characterized by the presence of abnormal genital development in a 46,XY individual with normal testis development and partial responsiveness to age-appropriate levels of androgens.
Refractory complex partial seizure with impairment of consciousness	An epileptic seizure originating within networks limited to one hemisphere with impaired awareness (defined as impairment of knowledge of self and environment) occurring at any point within the seizure, regardless of whether motor or nonmotor.
Refractory complex partial seizure with impairment of consciousness	Drug resistance to anti-seizure medication (disorder)
épilepsie partielle continue réfractaire	A prolonged focal-onset clonic seizure occurring and limited to specific parts of the body such as the hand, face, arm or leg.
épilepsie partielle continue réfractaire	Drug resistance to anti-seizure medication (disorder)
épilepsie réfractaire	Drug resistance to anti-seizure medication (disorder)
épilepsie réfractaire	A disease of the brain characterized by an enduring predisposition to generate epileptic seizures.
épilepsie réfractaire du lobe frontal	A type of focal epilepsy where all the seizures originate within the frontal lobe.
épilepsie réfractaire du lobe frontal	Drug resistance to anti-seizure medication (disorder)
Refractory generalized convulsive epilepsy	A type of epilepsy that presents with generalised tonic-clonic seizures usually between 10 and 25 years of age in an otherwise normal adolescent or adult. The generalised tonic-clonic seizures are typically provoked by sleep deprivation. Other seizure types do not occur. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram must show generalised epileptiform discharges or capture a generalised tonic-clonic seizure and have a normal background.
Refractory generalized convulsive epilepsy	A type of epilepsy with only generalised onset epileptic seizures.
Refractory generalized convulsive epilepsy	Drug resistance to anti-seizure medication (disorder)
épilepsie réfractaire généralisée non convulsive	A type of epilepsy with only generalised onset epileptic seizures.
épilepsie réfractaire généralisée non convulsive	Drug resistance to anti-seizure medication (disorder)
Refractory idiopathic generalized epilepsy	Drug resistance to anti-seizure medication (disorder)
Refractory idiopathic generalized epilepsy	A distinct sub-group of genetic generalised epilepsy that includes only four epilepsy syndromes: childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy, and epilepsy with generalised tonic-clonic seizures alone.
Refractory 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.
Refractory 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.
Refractory juvenile myoclonic epilepsy	Drug resistance to anti-seizure medication (disorder)
Refractory juvenile myoclonic epilepsy	A type of epilepsy that presents with myoclonic epileptic seizures, usually between 10 and 24 years of age, in an otherwise normal adolescent or adult. Generalized tonic-clonic seizures occur in greater than 90 percent of individuals and absence seizures occur in a third. Seizures typically occur shortly after waking and when tired. Sleep deprivation is an important provoking factor. Photosensitivity is common. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram shows 3 to 5.5 Hz generalized spike-wave and polyspike-wave and a normal background.
épilepsie focale réfractaire	A type of epilepsy with only focal onset epileptic seizures. Seizures can arise from a single location or multiple locations.
épilepsie focale réfractaire	Drug resistance to anti-seizure medication (disorder)
Refractory myoclonic epilepsy	Drug resistance to anti-seizure medication (disorder)
Refractory myoclonic epilepsy	A type of epilepsy with only generalised onset epileptic seizures.
Refractory occipital lobe epilepsy	Occipital lobe epilepsy
Refractory occipital lobe epilepsy	Drug resistance to anti-seizure medication (disorder)
Refractory parietal lobe epilepsy	Drug resistance to anti-seizure medication (disorder)
Refractory parietal lobe epilepsy	A type of focal epilepsy where all the seizures originate within the parietal lobe.
frigidità relativa	Orgasm incapacity
frigidità relativa	Sexual incompatibility
épilepsie non photosensible auto-induite	A disease of the brain characterized by an enduring predisposition to generate epileptic seizures.
épilepsie non photosensible auto-induite	Disorder in which the subject intentionally produces, feigns, falsifies or aggravates physical or psychological symptoms or injury.
Sexually acquired reactive arthropathy of the pelvic region and thigh	Sexually acquired reactive arthritis of joint of pelvic wall
Sexually acquired reactive arthropathy of the pelvic region and thigh	Reactive arthritis of joint of hip due to and following sexually transmitted disease (disorder)
Small visual image	Dissociative neurological symptom disorder with visual symptom (disorder)
Small visual image	Micropsia (disorder)
Status epilepticus due to generalized idiopathic epilepsy	A distinct sub-group of genetic generalised epilepsy that includes only four epilepsy syndromes: childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy, and epilepsy with generalised tonic-clonic seizures alone.
Status epilepticus due to generalized idiopathic epilepsy	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.
Status epilepticus due to intractable idiopathic generalized epilepsy	A distinct sub-group of genetic generalised epilepsy that includes only four epilepsy syndromes: childhood absence epilepsy, juvenile absence epilepsy, juvenile myoclonic epilepsy, and epilepsy with generalised tonic-clonic seizures alone.
Status epilepticus due to intractable idiopathic generalized epilepsy	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.
Status epilepticus due to refractory epilepsy	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.
Status epilepticus due to refractory epilepsy	A disease of the brain characterized by an enduring predisposition to generate epileptic seizures.
Status epilepticus due to refractory simple partial epilepsy	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.
Status epilepticus due to refractory simple partial epilepsy	A type of epilepsy with only focal onset epileptic seizures. Seizures can arise from a single location or multiple locations.
Status epilepticus in benign Rolandic epilepsy	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.
Status epilepticus in benign Rolandic epilepsy	A common type of self-limited focal epilepsy syndrome, which begins typically between four and ten years (peak is seven years; range three to twelve years). Seizures are focal, infrequent (most children have fewer than ten in lifetime), brief (typically less than two to three minutes) and occur mostly in sleep (eighty to ninety percent of children). Individuals may have frequent seizures over a few days or weeks and then several months before subsequent seizure. Focal seizures with characteristic frontoparietal opercular features and/or nocturnal bilateral tonic-clonic seizures are mandatory for diagnosis. Characteristic semiology includes somatosensory symptoms (unilateral numbness or paresthesia of the tongue, lips, gums and inner cheek), orofacial motor signs (unilateral tonic or clonic contractions), speech arrest (dysarthria or anarthria) with preserved understanding, and sialorrhea. Seizures may evolve rapidly to tonic-clonic activity of the ipsilateral upper limb, to an ipsilateral hemiclonic seizure, or to a focal to bilateral tonic-clonic seizure. Todd paresis may occur postictally. Seizures occurring during sleep are seen within one hour of falling asleep or one to two hours prior to awakening. Development and cognition are typically normal. Neurological examination is normal. The electroencephalogram (EEG) background activity is normal. EEG must show centrotemporal biphasic epileptiform discharges which are characteristically high-amplitude complexes (less than 200 microvolts, peak to trough) that activate in drowsiness and sleep. MRI is normal or has nonspecific findings.
cellules ethmoïdales moyennes	Structure of posterior cells of ethmoid sinus
cellules ethmoïdales moyennes	Structure of anterior cells of ethmoid sinus
artère nasale postérieure, latérale et septale	Structure of dorsal nasal artery
artère nasale postérieure, latérale et septale	Lateral nasal artery
abuso di sostanze	A specific, singular event or a short period in which substance use leads to damage to an individual's physical or mental health or results in behavior that causes physical or psychological harm to others. Health damage results from intoxication behaviors, direct or secondary toxic effects on body organs and system, or harmful method of substance intake. Harm to others encompasses any physical or mental harm directly attributable to the user's intoxicated behavior.
abuso di sostanze	A pattern of substance use that leads to damage to an individual's physical or mental health or results in behavior leading to physical or psychological harm to others. The pattern of substance use is observed for a minimum of 12 months for occasional use or at least one month for continuous use (daily or nearly daily). Health damage results from intoxication behaviors, direct or secondary toxic effects on body organs and system or harmful method of substance intake. Harm to others encompasses any physical or mental harm directly attributable to the user's intoxicated behavior.
épilepsie myoclonique symptomatique	A disease of the brain characterized by an enduring predisposition to generate epileptic seizures.
épilepsie myoclonique symptomatique	A type of epilepsy with only generalised onset epileptic seizures.
T3 and/or N1 (III): Fallopian tube tumor involves one or both tube(s) with peritoneal implants outside the pelvis and/or regional lymph node metastasis	American Joint Committee on Cancer cT3 (qualifier value)
T3 and/or N1 (III): Fallopian tube tumor involves one or both tube(s) with peritoneal implants outside the pelvis and/or regional lymph node metastasis	American Joint Committee on Cancer cN1 (qualifier value)
T3 and/or N1 (III): Ovarian tumor involves one or both ovaries with microscopically confirmed peritoneal metastasis outside the pelvis and/or regional lymph node metastasis	American Joint Committee on Cancer cT3 (qualifier value)
T3 and/or N1 (III): Ovarian tumor involves one or both ovaries with microscopically confirmed peritoneal metastasis outside the pelvis and/or regional lymph node metastasis	American Joint Committee on Cancer cN1 (qualifier value)
T3a,b: Colon/rectum tumor invades <=5 mm beyond the border of the muscularis propria	American Joint Committee on Cancer cT3a (qualifier value)
T3a,b: Colon/rectum tumor invades <=5 mm beyond the border of the muscularis propria	American Joint Committee on Cancer cT3b (qualifier value)
T3c,d: Colon/rectum tumor invades >5 mm beyond the border of the muscularis propria	American Joint Committee on Cancer cT3d (qualifier value)
T3c,d: Colon/rectum tumor invades >5 mm beyond the border of the muscularis propria	American Joint Committee on Cancer cT3c (qualifier value)
Teacher of the handicapped	Intellectual disability teacher
Teacher of the handicapped	Special education teacher
Tis: Carcinoma in situ, breast: Intraductal carcinoma, lobular carcinoma in situ, or Paget's disease of the nipple with no tumor	American Joint Committee on Cancer cTis(Paget) (qualifier value)
Tis: Carcinoma in situ, breast: Intraductal carcinoma, lobular carcinoma in situ, or Paget's disease of the nipple with no tumor	American Joint Committee on Cancer cTis(DCIS) (qualifier value)
Tis: Carcinoma in situ, breast: Intraductal carcinoma, lobular carcinoma in situ, or Paget's disease of the nipple with no tumor	American Joint Committee on Cancer cTis (qualifier value)
bronchographie transcricoïdienne	Computed tomography of bronchus with contrast (procedure)
bronchographie transcricoïdienne	Fluoroscopy of bronchus with contrast
bronchographie transcricoïde bilatérale	Fluoroscopy of bilateral bronchi with contrast
bronchographie transcricoïde bilatérale	CT of bilateral bronchi with contrast
bronchographie transglottique bilatérale	Fluoroscopy of bilateral bronchi with contrast
bronchographie transglottique bilatérale	CT of bilateral bronchi with contrast

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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)