FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.7  |  FHIR Version n/a  User: [n/a]

900000000000523009: 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)


49567 members. Search Members:

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
basiliximab 10 mg injektionsvæske (pulver til rekonstitution) + solvens Basiliximab 10 mg powder for solution for injection vial
basiliximab 20 mg injektionsvæske (pulver til rekonstitution) + solvens Basiliximab 20 mg powder for solution for injection vial
Basiliximab 20mg/vial powder Basiliximab 20 mg powder for solution for injection vial
Basophil count NOS Basophil count
Basophil count NOS Basophil count
Basophilic stippling Basophilic stippling
Battered baby &/or child syndrome NOS Battered baby AND/OR child syndrome
mistanke om, at spædbarn har været udsat for vold i hjemmet, familieanamnese Suspected victim of child abuse
Battered baby suspect - FH Suspected victim of child abuse
Battey disease Battey disease (disorder)
Bay area functional assessment Bay Area Functional Performance Evaluation (assessment scale)
Baylisascaris species Baylisascaris
Bcg live intravesical 120mg Bacillus Calmette-Guerin antigen-containing product
BCG levende120 mg intravesikal opløsning Bacillus Calmette-Guerin antigen-containing product
Bdellovibrio-art Bdellovibrio
Beaterman - paper (& [etc]) &/or board process Beater operator
Beaterman - paper (& [etc]) &/or board process Beaterman - paper etc
Beaterman - paper (& [etc]) &/or board process Beaterman - paper etc
Smukt udseende Finding of general observation of appearance
Becker muscular dystrophy Restrictive cardiomyopathy with endomyocardial fibrosis (disorder)
Becker muscular dystrophy Becker muscular dystrophy (disorder)
beclometasonforbindelser Beclometasone
beclometasonforbindelser Beclometasone dipropionate
beclometasondipropionat 100 µg indåndingsudløst tørpulverinhalator Beclometasone dipropionate 100 microgram/actuation powder for inhalation
beclometasondipropionat 200 µg indåndingsudløst tørpulverinhalator Beclometasone dipropionate 200 microgram/actuation powder for inhalation
Beclomethasone dipropionate 200micrograms breath-actuated dry powder inhaler Beclometasone dipropionate 200 microgram/actuation powder for inhalation
beclometasondipropionat 200 µg inhalator Beclomethasone dipropionate 200 microgram/actuation pressurized solution for inhalation
beclometasondipropionat 250 µg indåndingsudløst tørpulverinhalator Beclometasone dipropionate 250 microgram/actuation powder for inhalation
beclometasondipropionat 250 µg inhalator Beclomethasone dipropionate 250 microgram/actuation pressurized solution for inhalation
beclometasondipropionat 400 µg indåndingsudløst tørpulverinhalator Beclometasone dipropionate 400 microgram/actuation powder for inhalation
Beclomethasone dipropionate 400micrograms breath-actuated dry powder inhaler Beclometasone dipropionate 400 microgram/actuation powder for inhalation
beclometasondipropionat 50 µg vandig næsespray Beclometasone dipropionate 50 microgram/actuation nasal spray
beclometasondipropionat 50 µg indåndingsudløst tørpulverinhalator Beclometasone dipropionate 50 microgram/actuation powder for inhalation
beclometasondipropionat 50 µg inhalator Beclomethasone dipropionate 50 microgram/actuation pressurized solution for inhalation
Bed blanket, reusable Blanket, device (physical object)
Bed blanket, single-use Blanket, device (physical object)
Bed pillow, reusable Pillow
Bed pillow, single-use Pillow
Bed sheet, reusable Bed sheet, device (physical object)
Bed sheet, single-use Bed sheet, device (physical object)
Bedrail cover, reusable Bedrail cover
Bedrail cover, single-use Bedrail cover
Bedtime blood sugar (& level) Bedtime blood sugar measurement (procedure)
bistik uden reaktion Bee sting
Bee-eater Genus Merops (organism)
Bee-eater Family Meropidae (organism)
Beech pollen allergen Beech pollen
Beggiatoa-art Beggiatoa
Behr syndrome A rare neuro-ophthalmological disease associating the typical optic atrophy with other extra-ocular manifestations such as sensorineural deafness, myopathy, chronic progressive external ophthalmoplegia, ataxia and peripheral neuropathy. More rarely, other manifestations have been associated with this condition, such as spastic paraplegia or multiple-sclerosis like illness.
Behr syndrome Autosomal recessive spastic paraplegia type 55 (SPG 55) is a rare, complex type of hereditary spastic paraplegia characterized by childhood onset of progressive spastic paraplegia associated with optic atrophy (with reduced visual acuity and central scotoma), ophthalmoplegia, reduced upper-extremity strength and dexterity, muscular atrophy in the lower extremities, and sensorimotor neuropathy. SPG55 is caused by mutations in the C12ORF65 gene (12q24.31) encoding probable peptide chain release factor C12orf65, mitochondrial.
Behr syndrome 3-Methylglutaconic aciduria type 3
Behçet's syndrome Behcet's syndrome
Behçet's syndrome Generalized aphthosis
Beijerinckia-art Genus Beijerinckia (organism)
Bell's palsy &/or facial palsy Bell's palsy (disorder)
Bell's palsy &/or facial palsy Facial nerve disorder (disorder)
Bell's palsy &/or facial palsy Bell's palsy (disorder)
Bell's palsy &/or facial palsy Facial palsy
Bellbird Anthornis melanura (organism)
Bellbird Genus Procnias (organism)
ikke gammel nok til at kunne ræsonnere Finding related to ability to reason
Below elbow amputation (& Krukenberg) Amputation of forearm through radius AND ulna
Below knee amputation (& [Boyd] or [Burgess] or [Guyon]) Guyon amputation (procedure)
Below knee amputation (& [Boyd] or [Burgess] or [Guyon]) Amputation of lower limb (procedure)
Below knee-1-W-S stockings Stocking (physical object)
Below knee-2-W-S hose Stocking (physical object)
Belted kingfisher Megaceryle alcyon (organism)
Belzer UW cold storage solution Pharmaceutical / biologic product (product)
Belzer UW-opløsning til organnedkøling Pharmaceutical / biologic product (product)
bemiparinnatrium 12.500 IE/ml injektionsvæske, opløsning i fyldt injektionssprøjte a 0,2 ml Bemiparin sodium 12500 unit/mL solution for injection
bemiparinnatrium 17.500 IE/ml injektionsvæske, opløsning i fyldt injektionssprøjte a 0,2 ml Product containing precisely bemiparin sodium 17500 unit/1 milliliter conventional release solution for injection (clinical drug)
bemiparinnatrium 25.000 IE/ml injektionsvæske, opløsning i fyldt injektionssprøjte a 0,2 ml Bemiparin sodium 25000 unit/mL solution for injection
bendrofluazid 2,5 mg + kalium 7,7 mmol tablet med modificeret udløsning Product containing precisely bendroflumethiazide 2.5 milligram and potassium chloride 573 milligram/1 each prolonged-release oral tablet (clinical drug)
bendrofluazid 2,5 mg + kalium 8,4 mmol tablet med modificeret udløsning Product containing precisely bendroflumethiazide 2.5 milligram and potassium chloride 630 milligram/1 each prolonged-release oral tablet (clinical drug)
Benefit, allowance or pension: [sickness] or [invalidity] or [disablement] Sickness/invalidity benefit
Benefit, allowance or pension: [sickness] or [invalidity] or [disablement] Invalidity pension
Benefit, allowance or pension: [sickness] or [invalidity] or [disablement] Invalidity benefit
Benefit, allowance or pension: [sickness] or [invalidity] or [disablement] Sickness benefit
Bengal jungle babbler Jungle babbler
Benign (neoplasm) or (tumour) lip &/or oral &/or pharynx Benign neoplasm of pharynx
Benign (neoplasm) or (tumour) lip &/or oral &/or pharynx Benign neoplasm of oral cavity (disorder)
Benign (neoplasm) or (tumour) lip &/or oral &/or pharynx Benign neoplasm of oral cavity (disorder)
Benign (neoplasm) or (tumour) lip &/or oral &/or pharynx Benign neoplasm of lip
Benign (neoplasm) or (tumour) lip &/or oral &/or pharynx Benign neoplasm of lip
Benign (neoplasm) or (tumour) lip &/or oral &/or pharynx Benign neoplasm of mouth region (disorder)
Benign (neoplasm) or (tumour) lip &/or oral &/or pharynx Benign neoplasm of mouth region (disorder)
Benign (neoplasm) or (tumour) lip &/or oral &/or pharynx Benign neoplasm of lip, oral cavity and pharynx
benign acinærcelletumor Acinar cell tumour of uncertain behaviour
Benign autosomal dominant mikrocefali A rare genetic non-syndromic developmental defect during embryogenesis malformation syndrome with characteristics of congenital, non-progressive, occipitofrontal head circumference that is 2 or more standard deviations below the mean for age, gender and ethnicity which is associated with normal brain architecture and uncomplicated by other abnormalities. Borderline to moderate intellectual disability, as well as early psychomotor delay, may or may not be associated.
Benign autosomal dominant osteopetrose A rare sclerosing bone disorder characterized by skeletal densification that predominantly involves the cranial vault.
Benign autosomal dominant osteopetrose A sclerosing disorder of the skeleton characterized by increased bone density that classically displays the radiographic sign of sandwich vertebrae (dense bands of sclerosis parallel to the vertebral endplates).
Benign congenital hypotonia Benign congenital hypotonia
Benign congenital hypotonia Neonatal hypotonia
Benign kutan vaskulær tumor Vascular neoplasm of skin (disorder)
Benign kutan vaskulær tumor Hemangioma of skin
Benign essential tremor Hereditary essential tremor
Benign essential tremor Essential tremor
Benign familial tremor Hereditary essential tremor
Benign familial tremor Essential tremor
Benign familiær tremor Essential tremor
Benign familiær tremor Hereditary essential tremor

Start Previous Page 84 of 496 Next End


Reference Sets

Reference set descriptor

Back to Start