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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 glucocorticoid deficiency
Familial granulomatous inflammatory arthritis, dermatitis and uveitis
Familial haematuria
Familial hemiplegic migraine
Familial haemolytic uraemic syndrome
Familial haemophagocytic lymphohistiocytosis
Familial haemorrhagic diathesis
Familial hirsutism
Familial hyperaldosteronism
Familial hyperaldosteronism type 1
Familial hyperaldosteronism type 2
Familial hyperaldosteronism type 3
Familial hyperalphalipoproteinaemia
Familial hypercholanemia
Familial hypercholesterolaemia
Familial hypercholesterolaemia - heterozygous
Familial homozygous hypercholesterolaemia
Double heterozygous familial hypercholesterolaemia
Familial hypercholesterolaemia due to genetic defect of apolipoprotein B
Familial hypercholesterolaemia due to heterozygous LDL receptor mutation
Familial hypercholesterolaemia due to homozygous LDL receptor mutation
Familial hyperchylomicronaemia
Familial hypergastrinaemic duodenal ulcer
Familial hyperkalaemic periodic paralysis
Familial hyperlipoproteinaemia
Familial hyperprolactinaemia
Familial hyperthyroidism
Familial non-autoimmune autosomal dominant hyperthyroidism
Familial hypertriglyceridaemia
Familial hypertrophy of sphincter of Oddi
Familial hypertryptophanaemia
Familial hypoalphalipoproteinaemia
Familial hypobetalipoproteinaemia
Familial hypobetalipoproteinaemia - heterozygous form
Familial hypobetalipoproteinaemia - homozygous form
Familial hypocalciuric hypercalcaemia
Familial hypoceruloplasminaemia
Familial hypodontia
Familial hypokalaemic alkalosis, Gullner type
Familial hypokalemic and hypomagnesemic tubulopathy
Familial hypokalaemic periodic paralysis
Familial hypolipoproteinaemia
Familial hypomagnesaemia hypercalciuria nephrocalcinosis with severe ocular involvement
Familial hypomagnesaemia-hypercalciuria
Familial hypoplastic, glomerulocystic kidney
Familial penile hypospadias
Familial idiopathic dilatation of right atrium
Familial idiopathic hypercalciuria
Familial idiopathic pulmonary fibrosis
Familial IgA nephropathy
Familial immunoglobulin hypercatabolism
Familial infantile gigantism
Familial infantile myasthenia
Familial infantile myoclonic epilepsy
Familial interstitial nephritis
Familial intestinal malrotation
Familial isolated arrhythmogenic right ventricular dysplasia
Familial isolated clinodactyly of finger
Familial isolated complete right bundle branch block
Familial isolated congenital asplenia
Familial isolated hyperparathyroidism
Familial isolated hypoparathyroidism
Familial isolated pituitary adenoma
Familial isolated trichomegaly
Familial juvenile gout
Familial juvenile hypertrophy of the breast
Familial lichen amyloidosis
Familial lipoprotein deficiency
Hyperlipoproteinaemia, type I
Familial lipoprotein lipase deficiency with type I phenotype
Familial lipoprotein lipase deficiency with type V phenotype
Familial localised cutaneous amyloidosis
Familial male-limited precocious puberty
Familial malignant melanoma of skin
Familial malignant neoplasm of pancreas
Familial malignant neoplasm of prostate
Familial mastocytosis
Familial median cleft of upper and lower lip
Familial megalencephaly
Familial megaloblastic anaemia
Familial mesangial sclerosis
Familial mesial temporal lobe epilepsy with febrile seizures
Familial methaemoglobinaemia
Familial methionine malabsorption
Familial mitral valve prolapse
Familial multiple benign meningioma
Familial multiple cylindroma
Familial multiple factor deficiency syndrome
Familial multiple factor deficiency syndrome, type I
Familial multiple factor deficiency syndrome, type II
Familial multiple factor deficiency syndrome, type III
Familial multiple factor deficiency syndrome, type IV
Familial multiple factor deficiency syndrome, type V
Familial multiple factor deficiency syndrome, type VI
Familial multiple leiomyoma cutis
Familial multiple lipomata
Familial multiple lipomatosis
Familial multiple lipoprotein-type hyperlipidaemia
Familial multiple naevi flammei
Familial multiple pilomatrixoma
Familial multiple polyposis syndrome

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