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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
Hepatitis due to acquired toxoplasmosis
Hepatitis caused by adenovirus
Bacterial hepatitis
Hepatitis caused by sexually transmissible virus
Hepatitis due to infection
Hepatitis in coxsackie viral disease
Hepatitis in late syphilis
Hepatitis in secondary syphilis
Hepatitis in yellow fever
Hepatoblastoma
Hepatocellular dysplasia
Hepatocellular jaundice
Hepatocellular liver damage
Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
Hepatomegaly with AIDS (acquired immunodeficiency syndrome)
Hepatomphalocele
Hepatoportal microvascular dysplasia
Hepatoportal sclerosis
Hepatoptosis
Hepatopulmonary syndrome
Hepatorenal syndrome
Hepatorenal syndrome as a complication of care
Hepatorenal syndrome due to a procedure
Hepatorenal syndrome following delivery
Hepatosplenic T-cell lymphoma
Hepatosplenic gamma-delta cell lymphoma
Hepatosplenic schistosomiasis
Hepatosplenic schistosomiasis caused by Schistosoma haematobium
Hepatosplenomegaly
Heptachlor poisoning
Herbal medicine adverse reaction
Herbicide and/or fungicide poisoning
Herbicide poisoning
Hereditary angioedema - type 1
Hereditary angioedema - type 2
Hereditary acanthocytosis
Hereditary acantholytic dermatosis
Hereditary acrodermatitis enteropathica
Hereditary acrokeratotic poikiloderma of Weary
Hereditary acroosteolysis
Hereditary adrenal unresponsiveness to corticotropin
Hereditary amyloidosis
Familial anetoderma
Hereditary angioedema
Hereditary angioedema with normal C1 esterase inhibitor activity
Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome
Hereditary antithrombin III deficiency
Hereditary arterial and articular multiple calcification syndrome
Hereditary ataxia
Hereditary autonomic neuropathy
Hereditary benign acanthosis nigricans
Hereditary benign acanthosis nigricans with insulin resistance
Hereditary benign intraepithelial dyskeratosis
Hereditary benign telangiectasia
Hereditary bilateral optic atrophy
Hereditary breast and ovarian cancer syndrome
Hereditary camptodactyly
Hereditary neoplastic syndrome
Hereditary cavernous haemangioma of brain
Hereditary cerebellar degeneration
Hereditary cerebral amyloid angiopathy, Dutch type
Hereditary cerebral amyloid angiopathy, Icelandic type
Hereditary cerebral haemorrhage with amyloidosis
Hereditary cerebrovascular amyloidosis
Hereditary choroidal dystrophy
Hereditary clear cell renal cell carcinoma
Hereditary clubbing
Hereditary coagulation factor deficiency
Hereditary combined coagulation factor deficiency
Hereditary combined deficiency of vitamin K-dependent clotting factors
Hypo-and hypermelanotic cutaneous macules, retarded growth, intellectual disability syndrome
Hereditary coproporphyria
Hereditary corneal dystrophy
Hereditary cryohydrocytosis with normal stomatin
Hereditary cryohydrocytosis with reduced stomatin
Hereditary cutaneous vascular syndrome
Hereditary degenerative disease of central nervous system
Hereditary diffuse carcinoma of stomach
Hereditary diffuse crescentic glomerulonephritis
Hereditary diffuse endocapillary proliferative glomerulonephritis
Hereditary diffuse leukoencephalopathy with spheroids
Hereditary diffuse melanosis
Hereditary diffuse membranous glomerulonephritis
Hereditary diffuse mesangiocapillary glomerulonephritis
Hereditary diffuse palmoplantar keratoderma
Hereditary disease
Hereditary disease in family possibly affecting fetus
Hereditary disorder by system
Hereditary disorder of cellular element of blood
Hereditary disorder of endocrine system
Hereditary disorder of immune system
Hereditary disorder of lymphatic system
Hereditary disorder of musculoskeletal system
Hereditary disorder of nervous system
Hereditary disorder of the integument
Hereditary disorder of the urinary system
Hereditary disorder of the visual system
Hereditary dysautonomia with motor neuropathy
Hereditary dysfibrinogenaemia
Hereditary dysplasia of blood vessel
Hereditary dysplasminogenaemia

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