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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
Congenital fusion of sacroiliac joint
Congenital fusion of spine
Congenital fusion of testis
Congenital gastric perforation
Congenital gastrointestinal-urinary tract fistula
Congenital generalised alopecia
Congenital generalised flexion contractures of lower limb joints
Congenital generalised hypertrichosis
Congenital genu recurvatum
Congenital genu valgum
Congenital genu varum
Congenital genu varum of left knee
Congenital genu varum of right knee
Congenital gingival granular cell tumour
Congenital glaucoma
Congenital glaucoma of right eye
Congenital glenoid dysplasia
Congenital glottic web of larynx
Congenital glucose-galactose malabsorption
Congenital group A haemolytic streptococcal pneumonia
Congenital group B haemolytic streptococcal pneumonia
Congenital hallux valgus
Congenital hallux valgus of left great toe
Congenital hallux valgus of right great toe
Congenital hallux varus
Congenital hamartoma
Bilateral congenital hamartoma of irises
Congenital hamartoma of skin
Congenital hammer toe
Bilateral congenital hammer toes
Congenital hearing disorder
Congenital heart block
Sonoda syndrome
Congenital heart disease
Congenital heart disease in pregnancy
Congenital heart disease, septal and bulbar anomalies
Congenital haemangioma
Congenital hemihypertrophy
Congenital hemivertebra
Congenital haemolytic anaemia
Congenital haemolytic uraemic syndrome
Congenital haemorrhagic renal cyst
Congenital hepatic fibrosis
Congenital hepatitis A infection
Congenital hepatitis C infection
Congenital hepatomegaly
Congenital hereditary endothelial dystrophy
Corneal dystrophy and perceptive deafness syndrome
Congenital hereditary endothelial dystrophy type 1
Congenital hereditary endothelial dystrophy type 2
Congenital hereditary facial paralysis with variable hearing loss syndrome
Congenital hereditary muscular dystrophy
Congenital hernia of foramen of Morgagni
Congenital herpes simplex
Congenital heterochromia iridis
Congenital hiatus hernia
Developmental hip dysplasia
Congenital honeycomb lung
Congenital horizontal mandibular hyperplasia
Congenital horizontal mandibular hypoplasia
Congenital hourglass bladder
Congenital hourglass stomach
Congenital HIV infection
Congenital HIV positive status syndrome
Congenital human parvovirus infection
Congenital humeral varus
Congenital hydrocalicosis
Congenital hydrocele
Congenital hydrocele of canal of Nuck
Congenital hydrocephalus
Congenital hydrocephalus due to toxoplasmosis
Congenital hydronephrosis
Congenital hydronephrosis due to bladder obstruction
Congenital hydronephrosis due to ureteral obstruction
Congenital hydronephrosis due to ureteropelvic junction obstruction
Congenital hydrosalpinx
Congenital hydrothorax
Congenital hydroureter
Congenital hyperextension of limb
Congenital hyperflexion of limb
Congenital hypergammaglobulinaemia
Congenital hyperplasia of intrahepatic bile duct
Congenital hyperplasia of kidney
Congenital hyperplasia of lung
Congenital hyperplasia of muscle
Congenital hyperplasia of sebaceous glands of lip
Congenital hypertonia
Congenital hypertrichosis
Congenital hypertrichosis lanuginosa
Congenital hypertrophic pyloric stenosis
Congenital hypertrophy of adrenal gland
Congenital hypertrophy of aortic valve
Bilateral congenital lower limb hypertrophy
Congenital hypertrophy of cardiac ventricle
Congenital hypertrophy of fallopian tube
Congenital hypertrophy of lateral fold of hallux
Congenital hypertrophy of lung
Congenital hypertrophy of mitral valve
Congenital hypertrophy of nasal cavity
Congenital hypertrophy of ovary
Congenital hypertrophy of pulmonary valve

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