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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
2.5 year examination abnormal - referred
20p partial trisomy syndrome
20p12.3 microdeletion syndrome
20p13 microdeletion syndrome
20q partial trisomy
20q11.2 microduplication syndrome
20q13.33 microdeletion syndrome
21q partial distal trisomy
21q partial monosomy syndrome
21q partial trisomy
21q22.11q22.12 microdeletion syndrome
22q partial monosomy
22q partial trisomy
22q11.2 deletion syndrome
22q11.2 duplication syndrome
22q13.3 deletion syndrome
24 hour urine volume excessive
2p partial trisomy syndrome
2p13.2 microdeletion syndrome
2p15p16.1 microdeletion syndrome
2p21 microdeletion syndrome
2p21 microdeletion syndrome without cystinuria
2q partial trisomy syndrome
2q23.1 microdeletion syndrome
2q23.1 microduplication syndrome
2q24 microdeletion syndrome
2q31.1 microdeletion syndrome
2q32q33 microdeletion syndrome
2q33.1 microdeletion syndrome
3 beta-Hydroxysteroid dehydrogenase deficiency
3 point swing through gait
3 point swing to gait
3+ pitting oedema
3,3'-diiodothyronine level below reference range
3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
HMG COA reductase inhibitor adverse reaction
3-Hydroxyisobutyric aciduria
3-Ketoacyl-CoA triolase deficiency
3-Methylglutaconic aciduria
3-Methylglutaconic aciduria type 1
3-Methylglutaconic aciduria type 2
3-Methylglutaconic aciduria type 3
3-Methylglutaconic aciduria type 4
3-Methylglutaconic aciduria with normal 3-methylglutaconyl-CoA hydratase activity
3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency
3-Phosphoglycerate dehydrogenase deficiency
3-methylglutaconic aciduria type 5
3-methylglutaconic aciduria type 7
3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome
3-phosphoglycerate dehydrogenase deficiency infantile form
3-phosphoglycerate dehydrogenase deficiency juvenile form
3.5 year examination abnormal - on treatment
3p partial monosomy syndrome
3p partial trisomy syndrome
3q partial trisomy syndrome
3q13 microdeletion syndrome
3q26 microduplication syndrome
3q26q27 microdeletion syndrome
3q27.3 microdeletion syndrome
3q29 microdeletion syndrome
4 point gait
4+ pitting oedema
DNOC causing toxic effect
4-Hydroxyphenylpyruvate dioxygenase deficiency
4-aminopyridine poisoning
4-quinolones adverse reaction
4.5 year examination abnormal - for observation
4.5 year examination abnormal - on treatment
4.5 year examination abnormal - referred
46 XY disorder of sex development due to maternal ingestion of oestrogen
46,XX disorder of sex development due to maternal Krukenberg neoplasm
46,XX disorder of sex development due to maternal adrenal neoplasm
46,XX disorder of sex development due to maternal androluteoma
46,XX disorder of sex development due to maternal arrhenoblastoma
46,XX disorder of sex development with anorectal anomalies syndrome
46,XX disorder of sex development with skeletal anomalies syndrome
46,XY disorder of sex development due to maternal ingestion of progestogen
46,XY disorder of sex development, adrenal insufficiency due to CYP11A1 deficiency
46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome
46,XY ovotesticular disorder of sex development
46,XY partial gonadal dysgenesis
48,XYYY syndrome
49,XXXYY syndrome
49,XYYYY syndrome
4p partial monosomy syndrome
4p partial trisomy syndrome
4p16.3 microduplication syndrome
4q partial monosomy syndrome
4q partial trisomy syndrome
4q21 microdeletion syndrome
5,10-Methylenetetrahydrofolate reductase deficiency
5-HT3-receptor antagonist adverse reaction
5-HT3-receptor antagonist overdose
5-HT3-receptor antagonist poisoning
5-Oxoprolinase deficiency
5-amino-4-imidazole carboxamide ribosiduria
5-aminosalicylic acid adverse reaction
5-aminosalicylic acid overdose
5-aminosalicylic acid poisoning
5-HT secreting neuroendocrine tumour
5p partial monosomy syndrome

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