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1186921001: 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

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
4668054019 POSSIBLY REPLACED BY association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component
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
4668054019 POSSIBLY REPLACED BY association reference set en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT model component

782 members. Search Members:

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 Existential restriction modifier (core metadata concept)
Members targetComponentId
épilepsie partielle continue réfractaire Drug resistance to anti-seizure medication
épilepsie partielle continue réfractaire Epilepsia partialis continua (finding)
épilepsie réfractaire Drug resistance to anti-seizure medication
épilepsie réfractaire Epilepsy
épilepsie réfractaire Epilepsy
épilepsie réfractaire Drug resistance to anti-seizure medication
épilepsie réfractaire du lobe frontal Frontal lobe epilepsy (disorder)
épilepsie réfractaire du lobe frontal Drug resistance to anti-seizure medication
épilepsie réfractaire du lobe frontal Drug resistance to anti-seizure medication
épilepsie réfractaire du lobe frontal Frontal lobe epilepsy (disorder)
Refractory generalized convulsive epilepsy Drug resistance to anti-seizure medication
Refractory generalized convulsive epilepsy Generalized epilepsy
Refractory generalized convulsive epilepsy Epilepsy with generalised tonic-clonic seizures alone
Refractory generalized convulsive epilepsy Epilepsy with generalised tonic-clonic seizures alone
Refractory generalized convulsive epilepsy Generalized epilepsy
Refractory generalized convulsive epilepsy Drug resistance to anti-seizure medication
épilepsie réfractaire généralisée non convulsive Drug resistance to anti-seizure medication
épilepsie réfractaire généralisée non convulsive Drug resistance to anti-seizure medication
épilepsie réfractaire généralisée non convulsive Generalized epilepsy
épilepsie réfractaire généralisée non convulsive Generalized epilepsy
Refractory idiopathic generalized epilepsy Drug resistance to anti-seizure medication
Refractory idiopathic generalized epilepsy Idiopathic generalized epilepsy
Refractory idiopathic generalized epilepsy Drug resistance to anti-seizure medication
Refractory idiopathic generalized epilepsy Idiopathic generalized epilepsy
Refractory infantile spasms co-occurrent with status epilepticus Status epilepticus (finding)
Refractory infantile spasms co-occurrent with status epilepticus Status epilepticus (finding)
Refractory infantile spasms co-occurrent with status epilepticus Epileptic spasms
Refractory infantile spasms co-occurrent with status epilepticus Epileptic spasms
Refractory juvenile myoclonic epilepsy Juvenile myoclonic epilepsy
Refractory juvenile myoclonic epilepsy Drug resistance to anti-seizure medication
Refractory juvenile myoclonic epilepsy Drug resistance to anti-seizure medication
Refractory juvenile myoclonic epilepsy Juvenile myoclonic epilepsy
épilepsie focale réfractaire Drug resistance to anti-seizure medication
épilepsie focale réfractaire Focal epilepsy (disorder)
épilepsie focale réfractaire Drug resistance to anti-seizure medication
épilepsie focale réfractaire Focal epilepsy (disorder)
Refractory myoclonic epilepsy Drug resistance to anti-seizure medication
Refractory myoclonic epilepsy Generalized epilepsy
Refractory myoclonic epilepsy Drug resistance to anti-seizure medication
Refractory myoclonic epilepsy Generalized epilepsy
Refractory occipital lobe epilepsy Drug resistance to anti-seizure medication
Refractory occipital lobe epilepsy Drug resistance to anti-seizure medication
Refractory occipital lobe epilepsy A type of focal epilepsy where all the seizures originate within the occipital lobe.
Refractory occipital lobe epilepsy A type of focal epilepsy where all the seizures originate within the occipital lobe.
Refractory parietal lobe epilepsy Parietal lobe epilepsy
Refractory parietal lobe epilepsy Drug resistance to anti-seizure medication
Refractory parietal lobe epilepsy Parietal lobe epilepsy
Refractory parietal lobe epilepsy Drug resistance to anti-seizure medication
frigidité relative Sexual incompatibility
frigidité relative Sexual incompatibility
frigidité relative Orgasm incapacity (finding)
frigidité relative Orgasm incapacity (finding)
épilepsie non photosensible auto-induite Factitious disorder (disorder)
épilepsie non photosensible auto-induite Factitious disorder (disorder)
épilepsie non photosensible auto-induite Epilepsy
épilepsie non photosensible auto-induite Epilepsy
Sexually acquired reactive arthropathy of the pelvic region and thigh Reactive arthritis of joint of hip due to and following sexually transmitted disease (disorder)
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 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 Micropsia (disorder)
Small visual image Micropsia (disorder)
Small visual image Dissociative neurological symptom disorder with visual symptom (disorder)
Small visual image Dissociative neurological symptom disorder with visual symptom (disorder)
Status epilepticus due to complex partial epileptic seizure Status epilepticus mit komplexfokalen Anfällen
Status epilepticus due to complex partial epileptic seizure Focal onset impaired awareness epileptic seizure
Status epilepticus due to generalized idiopathic epilepsy Idiopathic generalized epilepsy
Status epilepticus due to generalized idiopathic epilepsy Status epilepticus (finding)
Status epilepticus due to generalized idiopathic epilepsy Status epilepticus (finding)
Status epilepticus due to generalized idiopathic epilepsy Idiopathic generalized epilepsy
Status epilepticus due to intractable idiopathic generalized epilepsy Idiopathic generalized epilepsy
Status epilepticus due to intractable idiopathic generalized epilepsy Status epilepticus (finding)
Status epilepticus due to intractable idiopathic generalized epilepsy Idiopathic generalized epilepsy
Status epilepticus due to intractable idiopathic generalized epilepsy Status epilepticus (finding)
Status epilepticus due to refractory complex partial seizures Focal onset impaired awareness epileptic seizure
Status epilepticus due to refractory complex partial seizures Status epilepticus mit komplexfokalen Anfällen
Status epilepticus due to refractory epilepsy Status epilepticus (finding)
Status epilepticus due to refractory epilepsy Epilepsy
Status epilepticus due to refractory epilepsy Epilepsy
Status epilepticus due to refractory epilepsy Status epilepticus (finding)
Status epilepticus due to refractory simple partial epilepsy Status epilepticus (finding)
Status epilepticus due to refractory simple partial epilepsy Focal epilepsy (disorder)
Status epilepticus due to refractory simple partial epilepsy Focal epilepsy (disorder)
Status epilepticus due to refractory simple partial epilepsy Status epilepticus (finding)
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.
Status epilepticus in benign Rolandic epilepsy Status epilepticus (finding)
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.
Status epilepticus in benign Rolandic epilepsy Status epilepticus (finding)
cellules ethmoïdales moyennes Structure of posterior cells of ethmoid sinus (body structure)
cellules ethmoïdales moyennes Structure of anterior cells of ethmoid sinus
cellules ethmoïdales moyennes Structure of posterior cells of ethmoid sinus (body structure)
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 Structure of dorsal nasal artery
artère nasale postérieure, latérale et septale Lateral nasal artery
artère nasale postérieure, latérale et septale Lateral nasal artery
abuso di sostanze Episode of harmful substance use
abuso di sostanze Episode of harmful substance use
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.
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 Epilepsy

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