FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  FHIR Version n/a  User: [n/a]

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
Hereditary dysplasminogenaemia
Hereditary elevated factor VIII
Hereditary elevated factor XI
Hereditary elliptocytosis
Hereditary elliptocytosis due to abnormal protein 4.1
Hereditary elliptocytosis due to alpha spectrin defect
Hereditary elliptocytosis due to beta spectrin defect in self-association
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction
Hereditary elliptocytosis due to deficiency of protein 4.1
Hereditary elliptocytosis due to glycophorin C deficiency
Hereditary elliptocytosis with transient poikilocytosis
Hereditary eosinophilia
Hereditary erythrokeratolysis
Hereditary essential tremor
Hereditary factor I deficiency disease
Hereditary factor II deficiency disease
Hereditary factor IX deficiency disease
Hereditary factor IX deficiency disease with inhibitor
Hereditary factor IX deficiency disease without inhibitor
Hereditary factor V deficiency disease
Hereditary factor VII deficiency disease
Hereditary factor VIII deficiency disease
Hereditary factor VIII deficiency disease with inhibitor
Hereditary factor VIII deficiency disease without inhibitor
Hereditary factor X deficiency disease
Hereditary factor XI deficiency disease
Hereditary factor XII deficiency disease
Hereditary factor XIII A subunit and B subunit deficiency
Hereditary factor XIII A subunit deficiency
Hereditary factor XIII B subunit deficiency
Hereditary factor XIII deficiency disease
Hereditary fibrosing poikiloderma, tendon contractures, myopathy, pulmonary fibrosis syndrome
Hereditary focal and segmental glomerular lesions
Hereditary folate deficiency anaemia
Hereditary follicular keratoses
Hereditary gastrogenic lactose intolerance
AGel amyloidosis
Hereditary geniospasm
Hereditary gingival fibromatosis
Hereditary glucocorticoid resistance
Hereditary hearing loss
Hereditary haemochromatosis
Hereditary haemoglobin S
Hereditary haemoglobinopathy
Hereditary haemoglobinopathy due to globin chain mutation
Hereditary haemolytic anaemia
Hereditary heparin cofactor II deficiency
Hereditary hollow viscus myopathy
Hereditary hypercarotenaemia and vitamin A deficiency
Hereditary hyperekplexia
Hereditary hyperfibrinogenaemia
Hereditary hyperhomocysteinemia
Hereditary hypermelanosis
Hereditary hypersegmentation
Hereditary hypertrophic neuropathy with paraproteinaemia
Hereditary hypertyrosinaemia
Hereditary hypophosphataemic rickets with hypercalciuria
Hereditary hypoplasminogenaemia
Hereditary hypotrichosis simplex
Hereditary hypotrichosis simplex of scalp
Hereditary hypotrichosis with recurrent skin vesicles syndrome
Hereditary inclusion body myopathy type 4
Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome
Hereditary insensitivity to pain with anhidrosis
Hereditary isolated aplastic anaemia
Hereditary isolated hypoparathyroidism due to agenesis of parathyroid gland
Hereditary isolated hypoparathyroidism due to impaired parathormone secretion
Hereditary keratoacanthoma
Hereditary left optic atrophy
Hereditary liability to pressure palsies
Hereditary lymphoedema
Hereditary lymphoedema and yellow nails
Hereditary lymphoedema type I
Hereditary lymphoedema type II
Hereditary macular dystrophy
Haemoglobin M disease
Hereditary minor glomerular abnormality
Hereditary mixed polyposis syndrome
Hereditary motor and sensory neuropathy
Hereditary motor and sensory neuropathy Okinawa type
Hereditary motor and sensory neuropathy type 5
Hereditary motor and sensory neuropathy with acrodystrophy
Hereditary motor and sensory neuropathy with optic atrophy
Hereditary motor and sensory neuropathy with retinitis pigmentosa
Hereditary motor end-plate disease
Hereditary motor neuron disease
Hereditary mucoepithelial dysplasia
Hereditary myopathy associated with hydrocephalus
Hereditary myopathy limited to females
Hereditary proximal myopathy with early respiratory failure
Hereditary nephritis
Hereditary nephrogenic diabetes insipidus
Hereditary nephropathy
Hereditary nephropathy co-occurrent with membranoproliferative glomerulonephritis type III
Hereditary neuraxial oedema
Hereditary neurocutaneous angiomata
Hereditary neutrophilia
Hereditary nonpolyposis colon cancer
Hereditary nonspherocytic haemolytic anaemia
Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity
HNSHA due to diphosphoglycerate mutase deficiency

Start Previous Page 410 of 901 Next End


Reference Sets

Reference set descriptor

Back to Start