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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
Autosomal dominant limb girdle muscular dystrophy type 1G
Autosomal dominant limb-girdle muscular dystrophy type 1H
Autosomal dominant macrothrombocytopenia
Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 1 deficiency
Autosomal dominant mendelian susceptibility to mycobacterial disease due to partial interferon gamma receptor 2 deficiency
Autosomal dominant multiple pterygium syndrome
Autosomal dominant muscular dystrophy not predominantly limb girdle
Autosomal dominant muscular dystrophy with gene located at 5q31
Autosomal dominant muscular dystrophy with limb girdle distribution
Autosomal dominant myoglobinuria
Autosomal dominant neovascular inflammatory vitreoretinopathy
Autosomal dominant nocturnal frontal lobe epilepsy
Autosomal dominant omodysplasia
Autosomal dominant optic atrophy and cataract
Autosomal dominant optic atrophy and peripheral neuropathy syndrome
Autosomal dominant optic atrophy classic form
Autosomal dominant optic atrophy plus syndrome
Autosomal dominant osteopetrosis type 2
Autosomal dominant palmoplantar keratoderma and congenital alopecia
Autosomal dominant polycystic kidney disease
Autosomal dominant polycystic kidney disease in childhood
Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis
Autosomal dominant popliteal pterygium syndrome
Autosomal dominant primary hypomagnesaemia with hypocalciuria
Autosomal dominant primary microcephaly
Autosomal dominant prognathism of mandible
Autosomal dominant progressive external ophthalmoplegia
Autosomal dominant progressive nephropathy with hypertension
Autosomal dominant pseudoxanthoma elasticum
Autosomal dominant pterygium of conjunctiva
Autosomal dominant retinitis pigmentosa
Autosomal dominant rhegmatogenous retinal detachment
Autosomal dominant secondary polycythaemia
Autosomal dominant sensory neuropathy
Autosomal dominant severe congenital neutropaenia
Autosomal dominant slowed nerve conduction velocity
Autosomal dominant spastic ataxia type 1
Autosomal dominant spastic paraplegia type 10
Autosomal dominant spastic paraplegia type 12
Autosomal dominant spastic paraplegia type 13
Silver disease
Autosomal dominant spastic paraplegia type 19
Autosomal dominant spastic paraplegia type 29
Autosomal dominant spastic paraplegia type 3
Autosomal dominant spastic paraplegia type 31
Autosomal dominant spastic paraplegia type 36
Autosomal dominant spastic paraplegia type 37
Autosomal dominant spastic paraplegia type 38
Autosomal dominant spastic paraplegia type 4
Autosomal dominant spastic paraplegia type 41
Autosomal dominant spastic paraplegia type 42
Autosomal dominant spastic paraplegia type 6
Autosomal dominant spastic paraplegia type 8
Autosomal dominant spondylocostal dysostosis
Autosomal dominant striatal neurodegeneration
Autosomal dominant tubulointerstitial kidney disease
Autosomal dominant variant form of albumin
Autosomal dominant vitreoretinochoroidopathy
Autosomal duplication
Autosomal hereditary disorder
Autosomal recessive axonal Charcot-Marie-Tooth disease type 2K
Autosomal recessive amelia
Recessive aplasia cutis congenita of limbs
Autosomal recessive asexual dwarfism
Autosomal recessive ataxia due to ubiquinone deficiency
Autosomal recessive axonal neuropathy with neuromyotonia
Autosomal recessive bestrophinopathy
Autosomal recessive brachyolmia
Verloes Bourguignon syndrome
Autosomal recessive centronuclear myopathy
Autosomal recessive cerebellar ataxia Beauce type
Autosomal recessive cerebellar ataxia due to STUB1 deficiency
Autosomal recessive cerebellar ataxia with late-onset spasticity
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2
Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUBCN deficiency
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency
Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency
Autosomal recessive cerebellar ataxia, psychomotor delay syndrome
Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome
Autosomal recessive cerebelloparenchymal disorder type 3
Autosomal recessive cerebral atrophy
Autosomal recessive chorioretinopathy and microcephaly syndrome
Autosomal recessive congenital methaemoglobinaemia
Autosomal recessive congenital methaemoglobinaemia type I
Autosomal recessive congenital methaemoglobinaemia type II
Autosomal recessive cutis laxa type 2A
Autosomal recessive cutis laxa type 2B
Autosomal recessive distal osteolysis syndrome
Autosomal recessive distal spinal muscular atrophy type 3
Autosomal recessive dopa responsive dystonia
Autosomal recessive dyskeratosis congenita
Autosomal recessive exfoliative ichthyosis
Autosomal recessive faciodigitogenital syndrome
Autosomal recessive familial woolly hair
Autosomal recessive focal segmental glomerulosclerosis
Autosomal recessive frontotemporal pachygyria
Autosomal recessive hereditary disorder
Autosomal recessive hyper-IgM syndrome
Autosomal recessive hyperinsulinism due to Kir6.2 deficiency

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