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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
Autonomic disorder co-occurrent and due to Chagas disease
Autonomic disorder of glossopharyngeal nerve
Autonomic dysreflexia
Autonomic facial cephalgia
Autonomic ganglionopathy
Autonomic hyperreflexia of bladder
Autonomic nerve injury
Autonomic nervous system disorder co-occurrent and due to neurodegenerative disorder
Autonomic nervous system drug overdose
Autonomic nervous system hyperactivity
Autonomic neuropathy
Autonomic neuropathy due to Allgrove syndrome
Autonomic neuropathy due to Fabry disease
Autonomic neuropathy due to Refsum Disease
Autonomic neuropathy due to Tangier disease
Autonomic neuropathy due to amyloidosis
Autonomic neuropathy due to diabetes mellitus
Autonomic neuropathy due to disorder of immune function
Autonomic neuropathy due to endocrine disease
Autonomic neuropathy due to medication induced hypoglycaemia
Autonomic neuropathy due to metabolic disease
Autonomic neuropathy due to sodium channelopathy
Autonomic neuropathy due to type 1 diabetes mellitus
Autonomic neuropathy due to type 2 diabetes mellitus
Autonomous thyroid function
Autonomously functioning thyroid goitre
Autoscopic hallucination
Autositic twin of asymmetrical conjoined twins
Autosomal agammaglobulinaemia with absent B-cells
Autosomal aneuploidy
Autosomal chromosomal disorder
Autosomal deletion - mosaicism
Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation
Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons
Autosomal dominant Charcot-Marie-Tooth disease type 2A1
Autosomal dominant Charcot-Marie-Tooth disease type 2A2
Autosomal dominant Charcot-Marie-Tooth disease type 2B
Autosomal dominant Charcot-Marie-Tooth disease type 2C
Autosomal dominant Charcot-Marie-Tooth disease type 2D
Autosomal dominant Charcot-Marie-Tooth disease type 2E
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Autosomal dominant Charcot-Marie-Tooth disease type 2G
Autosomal dominant Charcot-Marie-Tooth disease type 2I
Autosomal dominant Charcot-Marie-Tooth disease type 2J
Autosomal dominant Charcot-Marie-Tooth disease type 2K
Autosomal dominant Charcot-Marie-Tooth disease type 2L
Autosomal dominant Charcot-Marie-Tooth disease type 2M
Autosomal dominant Charcot-Marie-Tooth disease type 2N
Autosomal dominant Charcot-Marie-Tooth disease type 2O
Autosomal dominant Charcot-Marie-Tooth disease type 2Q
Autosomal dominant Charcot-Marie-Tooth disease type 2U
Autosomal dominant Emery-Dreifuss muscular dystrophy
Autosomal dominant adult-onset proximal spinal muscular atrophy
Autosomal dominant aplasia and myelodysplasia
Autosomal dominant beta2-microglobulinic amyloidosis
Autosomal dominant brachyolmia
Autosomal dominant centronuclear myopathy
Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome
Spinal muscular atrophy with lower extremity predominance
Autosomal dominant congenital benign spinal muscular atrophy
Autosomal dominant cystoid macular oedema
Autosomal dominant deficiency of plasminogen
Autosomal dominant diffuse palmoplantar keratoderma Norrbotten type
Autosomal dominant dopa responsive dystonia
Autosomal dominant dyskeratosis congenita
Autosomal dominant epidermolysis bullosa simplex
Autosomal dominant epilepsy with auditory features
Autosomal dominant excess of transthyretin
Autosomal dominant familial woolly hair
Autosomal dominant focal dystonia DYT25 type
Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering
Autosomal dominant focal segmental glomerulosclerosis
Autosomal dominant hereditary disorder
Haemochromatosis type 4
Autosomal dominant hereditary spastic paraplegia
Autosomal dominant hyperinsulinism due to Kir6.2 deficiency
Autosomal dominant hyperinsulinism due to SUR1 deficiency
Autosomal dominant hypocalcaemia
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome
Autosomal dominant hypophosphataemic bone disease
Autosomal dominant hypophosphataemic rickets
Autosomal dominant ichthyosis
Autosomal dominant ichthyosis vulgaris
Autosomal dominant idiopathic familial dystonia
Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
Autosomal dominant intermediate Charcot-Marie-Tooth disease type C
Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E
Autosomal dominant intermediate Charcot-Marie-Tooth disease type F
Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain
Autosomal dominant keratitis
Autosomal dominant lamellar ichthyosis
Autosomal dominant late onset Parkinson disease
Autosomal dominant late onset basal ganglia degeneration
Autosomal dominant late-onset retinal degeneration
Autosomal dominant limb girdle muscular dystrophy type 1A
Autosomal dominant limb girdle muscular dystrophy type 1D
Autosomal dominant limb girdle muscular dystrophy type 1E
Autosomal dominant limb girdle muscular dystrophy type 1F
Autosomal dominant limb girdle muscular dystrophy type 1G

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