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1244621000168103: Australian emergency department reference set (foundation metadata concept)


Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED Clinical Terms Australian extension

Descriptions:

Id Description Lang Type Status Case? Module
3194481000168117 Australian emergency department reference set (foundation metadata concept) en Fully specified name Active Case sensitive SNOMED Clinical Terms Australian extension
3194491000168119 Australian emergency department reference set en Synonym Active Case sensitive SNOMED Clinical Terms Australian extension
3194501000168114 Australian EDRS (emergency department reference set) en Synonym Active Case sensitive SNOMED Clinical Terms Australian extension
4351711000168117 <p>Supports the recording of reasons for presentation, presenting problems and diagnoses within emergency department settings in Australia.&nbsp;</p><p>It supersedes and expands on the content of the earlier Emergency Department Reference Set (EDRS) suite to provide a wide range of clinically relevant terms to enable safe clinical care delivery, a capability to serve clinician decision support, care guidelines and pathways, and provide interoperability with inpatient and general practice records when patients transferred between care settings.</p><p>This reference set supports the accurate and unambiguous electronic communication and exchange of information between clinicians involved in a patient's care relating to that patient's presentation at the point of triage and diagnosis at the point of discharge from an Emergency department.</p><p><b>Target client: </b>NCTS</p> en Definition Active Case sensitive SNOMED Clinical Terms Australian extension


90032 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Australian emergency department reference set Is a Emergency department clinical group true Inferred relationship Some
Australian emergency department reference set Is a Simple type reference set true Inferred relationship Some
Australian emergency department reference set Developed by Australian Digital Health Agency true Inferred relationship Some 1937751348
Australian emergency department reference set Has licence SNOMED CT-AU licence​ true Inferred relationship Some 1188790823

Members
Familial multiple polyposis syndrome
Familial multiple syringomata
Familial multiple trichoepitheliomata
Familial myoclonus of cerebral cortex
Familial nasal acilia
Familial neonatal seizures
Familial neoplastic disease
Familial neutropenia
Familial non-neuropathic amyloidosis
Familial non-obstructive reflux-associated chronic pyelonephritis
Familial nonmedullary thyroid carcinoma
Familial normokalaemic periodic paralysis
Familial obesity
Familial omphalocele syndrome with facial dysmorphism
Familial osteoarthropathy of the fingers
Familial osteochondritis dissecans
Familial osteodysplasia Anderson type
Familial painful callosities
Familial papillary thyroid carcinoma with renal papillary neoplasia syndrome
Familial paroxysmal rhabdomyolysis
Familial partial lipodystrophy
Familial partial lipodystrophy Kobberling type
Familial partial lipodystrophy Dunnigan type
Familial pericarditis
Familial periodic paralysis
Familial pigmented purpuric eruption
Familial platelet syndrome with predisposition to acute myelogenous leukaemia
Familial polycythaemia vera
Familial porphyria cutanea tarda
Familial hyperparathyroidism
Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement
Familial primary hypomagnesaemia with normocalciuria
Familial primary hypomagnesaemia with normocalciuria and normocalcaemia
Familial primary pulmonary hypertension
Familial progressive hyperpigmentation
Familial progressive hyperpigmentation and hypopigmentation of skin
Familial proximal renal tubular acidosis
Familial pseudohyperkalaemia
Familial pseudoinflammatory macular degeneration
Familial psoriasis
Familial psoriasis with affected first degree relative
Familial psoriasis without affected first degree relative
Familial pulmonary capillary haemangiomatosis
Familial recurrent peripheral facial palsy
Familial renal cell carcinoma
Familial renal glucosuria
Familial renal hypouricaemia
Familial renal iminoglycinuria
Familial restrictive cardiomyopathy
Familial scaphocephaly syndrome McGillivray type
Familial short stature
Familial sick sinus syndrome
Familial spontaneous pneumothorax
Familial steroid-resistant nephrotic syndrome with sensorineural deafness
Familial supernumerary nipple
Familial temporal lobe epilepsy
Familial thoracic aortic aneurysm and aortic dissection
Familial thrombocytosis
Familial thrombomodulin anomalies
Familial thyroglossal duct cyst
Familial thyroid dyshormonogenesis
Familial type 3 hyperlipoproteinaemia
Familial type 5 hyperlipoproteinaemia
Familial ventricular tachycardia
Familial vesicoureteral reflux
Familial visceral amyloidosis, Ostertag type
Familial visceral neuropathy
Familial x-linked hypophosphataemic vitamin D refractory rickets
Family Asclepiadaceae poisoning
Family Liliaceae poisoning
Family Rutaceae poisoning
Family Sapindaceae poisoning
Family Zamiaceae poisoning
Family aizoaceae poisoning
Family amaranthaceae poisoning
Family anacardiaceae poisoning
Family apiaceae poisoning
Family apocynaceae poisoning
Family araceae poisoning
Family araliaceae poisoning
Family asteraceae poisoning
Family berberidaceae poisoning
Family bereavement
Family boraginaceae poisoning
Family brassicaceae poisoning
Family buxaceae poisoning
Family cactaceae poisoning
Family cannabaceae poisoning
Family caryophyllaceae poisoning
Family chenopodiaceae poisoning
Family clusiaceae poisoning
Family combretaceae poisoning
Family conflict
Family convolvulaceae poisoning
Family crassulaceae poisoning
Family cucurbitaceae poisoning
Family cupressaceae poisoning
Family cycadaceae poisoning
Family dichapetalaceae poisoning
Family difficulty with crying infant
Family disruption

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