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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
Severe adrenal insufficiency
Severe alcohol dependence
Severe anxiety (panic)
Severe aortic valve regurgitation
Severe asthma
Severe biliary tract dysplasia
Severe bipolar I disorder
Severe bipolar I disorder, single manic episode with psychotic features
Severe bipolar I disorder, single manic episode with psychotic features, mood-congruent
Severe bipolar I disorder, single manic episode with psychotic features, mood-incongruent
Severe bipolar I disorder, single manic episode without psychotic features
Severe bipolar II disorder
Severe bipolar II disorder, most recent episode major depressive with psychotic features
Severe bipolar II disorder, most recent episode major depressive with psychotic features, mood-congruent
Severe bipolar II disorder, most recent episode major depressive with psychotic features, mood-incongruent
Severe bipolar II disorder, most recent episode major depressive without psychotic features
Severe bipolar II disorder, most recent episode major depressive, in full remission
Severe bipolar II disorder, most recent episode major depressive, in partial remission
Severe bipolar II disorder, most recent episode major depressive, in remission
Severe bipolar disorder
Severe bipolar disorder with psychotic features
Severe bipolar disorder with psychotic features, mood-congruent
Severe bipolar disorder with psychotic features, mood-incongruent
Severe bipolar disorder without psychotic features
Severe birth asphyxia
Severe birth asphyxia - Apgar score less than 4 at 1 minute
Severe birth asphyxia, Apgar 0-3
Severe bodily distress disorder
Severe bone marrow hyperplasia
Severe childhood autosomal recessive muscular dystrophy
Severe COPD
Severe chronic ulcerative colitis
Severe cognitive impairment
T-cell negative B-cell positive severe combined immunodeficiency due to JAK3 deficiency
Severe combined immunodeficiency disease
SCID due to absent T cell receptor
SCID due to absent adenosine deaminase
SCID due to absent class II HLA antigens
SCID due to absent IL-2 production
SCID due to absent IL-2 receptor
SCID due to absent lymphoid stem cells
SCID due to absent peripheral T cell maturation
Severe combined immunodeficiency due to CARD11 deficiency
Severe combined immunodeficiency due to complete RAG1 and/or RAG2 deficiency
Severe combined immunodeficiency due to CTPS1 deficiency
Severe combined immunodeficiency due to DCLRE1C deficiency
Severe combined immunodeficiency due to DNA dependent protein kinase catalytic subunit deficiency
Severe combined immunodeficiency due to IKK2 deficiency
Severe combined immunodeficiency due to LCK deficiency
Omenn syndrome
Severe combined immunodeficiency with low T- and B-cell numbers
Severe combined immunodeficiency with low or normal B-cell numbers
Severe combined immunodeficiency with maternofetal engraftment
Severe combined immunodeficiency with reticular dysgenesis
Cernunnos-XLF deficiency
Severe congenital hypochromic anaemia with ringed sideroblasts
Severe controlled persistent asthma
Severe crushing injury of abdominal organs
Severe crushing injury of abdominal organs with open wound into cavity
Severe crushing injury of abdominal organs without open wound into cavity
Severe cytopenia
Severe dehydration
Severe depressed bipolar I disorder
Severe depressed bipolar I disorder with psychotic features
Severe depressed bipolar I disorder with psychotic features, mood-congruent
Severe depressed bipolar I disorder with psychotic features, mood-incongruent
Severe depressed bipolar I disorder without psychotic features
Severe depression
Severe dermatitis, multiple allergies, metabolic wasting syndrome
Severe diarrhoea
Severe dry skin
Severe dyskaryosis on cervical smear cannot exclude invasive carcinoma
Severe dysplasia of colon
Severe dysplasia of rectum
Severe early childhood onset retinal dystrophy
Severe early-onset axonal neuropathy due to mitofusin 2 deficiency
Severe early-onset obesity insulin resistance syndrome due to SH2B1 deficiency
Severe oesophageal dysplasia
Severe expressive language delay
Severe feeding difficulties, failure to thrive, microcephaly due to ASXL3 deficiency syndrome
Severe fever with thrombocytopenia syndrome virus
Severe generalised recessive dystrophic epidermolysis bullosa
Severe gingivitis
Severe hearing loss
Severe hereditary factor IX deficiency disease with inhibitor
Severe hereditary factor IX deficiency disease without inhibitor
Severe hereditary factor VIII deficiency disease
Severe hereditary factor VIII deficiency disease with inhibitor
Severe hereditary factor VIII deficiency disease without inhibitor
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
Severe hereditary spherocytosis due to spectrin deficiency
Severe hyperemesis gravidarum
Diabetic severe hyperglycaemia
Severe hyperstimulation of ovaries
Severe hypokinesis of cardiac wall
Severe hypothyroidism
Severe hypoxic ischaemic encephalopathy
Severe hypoxic ischaemic encephalopathy of newborn
Severe ichthyoses
Severe idiopathic hypercalcaemia of infancy
Severe intellectual disability

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