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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
False labour pains
False memories
False passage of ureter
False perception
False positive complement fixation test for syphilis
False recognition
False tendon - heart
False-positive serological test for syphilis
Falsification
Falx laceration
Famciclovir adverse reaction
Familial Alzheimer's disease of early onset
Familial Alzheimer's disease of late onset
Familial Alzheimer-like prion disease
Familial C3B inhibitor deficiency syndrome
Familial Creutzfeldt-Jakob
Familial Mediterranean fever
Familial Ménière disease
Familial Scheuermann disease
Familial abdominal aortic aneurysm
Familial absence of villi
Familial acantholysis
Familial actinic prurigo of lip
Familial acute necrotising encephalopathy
Familial acute pancreatitis
Familial adrenal hypoplasia with absent pituitary luteinising hormone
Familial adrenocortical hypoplasia
Familial advanced sleep phase syndrome
Familial hypoaldosteronism
Familial alpha>2< adrenergic receptor defect in platelets
Familial amyloid nephropathy with urticaria AND deafness
Familial amyloid polyneuropathy
Familial amyloid polyneuropathy with cutaneous amyloidosis
Familial amyloid polyneuropathy, Iowa type
Familial amyloid polyneuropathy, Jewish type
Familial amyloid polyneuropathy, type II
Familial amyloid polyneuropathy, type VI
Familial angiolipomatosis
Familial annular erythema
Familial aplasia of the vermis
Familial apolipoprotein C-II deficiency
Familial arthrogryposis-cholestatic hepatorenal syndrome
Familial atrial fibrillation
Familial atrial myxoma
Familial avascular necrosis of head of femur
Familial benign copper deficiency
Familial benign flecked retina
Familial benign pemphigus
Familial bicuspid aortic valve
Familial cancer of breast
Familial cardiomyopathy
Familial caudal dysgenesis
Familial central diabetes insipidus
Familial cerebral saccular aneurysm
Familial cervical artery dissection
Familial chondrocalcinosis
Familial chondromalacia of patella
Familial chronic mucocutaneous candidiasis
Familial chronic mucocutaneous candidiasis - dominant type
Familial chronic mucocutaneous candidiasis - late onset type
Familial chronic mucocutaneous candidiasis - recessive type
Familial chronic pancreatitis
Familial cold urticaria
Familial combined hyperlipidaemia
Familial congenital mirror movements
Familial congenital palsy of trochlear nerve
Familial cutaneous collagenoma
Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome
Familial defective apolipoprotein B-100
ABri amyloidosis
ADan amyloidosis
Familial developmental dysphasia
Familial diabetes insipidus
Familial digital arthropathy and brachydactyly syndrome
Familial dilated cardiomyopathy with conduction defect due to lamin A/C mutation
Familial disease
Familial disease with storage of sterols (other than cholesterol)
Familial duodenal ulcer associated with rapid gastric emptying
Familial dysalbuminaemic hyperthyroxinaemia
Familial dysautonomia
Familial dyshormonogenetic goitre
Familial dyskeratotic comedones
Familial dyskinesia and facial myokymia
Familial encephalopathy with neuroserpin inclusion bodies
Familial eosinophilia
Familial episodic pain syndrome
Familial erythrocytosis
Familial erythrocytosis due to diphosphoglycerate mutase deficiency
Familial essential myoclonus
Familial expansile osteolysis
Familial extra unidentified structurally abnormal chromosome
Familial exudative vitreoretinopathy
Familial facial nerve palsy
Familial febrile convulsions
Familial febrile urticaria
Familial fibrous mediastinitis
Familial focal epilepsy with variable foci
Familial generalised lentiginosis
Familial gestational hyperthyroidism
Familial glomus tumour of skin
Familial glucocorticoid deficiency

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