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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
HNSHA due to diphosphoglycerate mutase deficiency
HNSHA due to gamma glutamyl cysteine synthetase deficiency
HNSHA due to glucose phosphate isomerase deficiency
HNSHA due to glutathione reductase deficiency
HNSHA due to glutathione synthetase deficiency
HNSHA due to hexokinase deficiency
Haemolytic anaemia due to erythrocyte adenosine deaminase overproduction
HNSHA due to phosphofructokinase deficiency
HNSHA due to phosphoglycerate kinase deficiency
HNSHA due to pyrimidine-5'-nucleotidase deficiency
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency
HNSHA due to NADH diaphorase deficiency
HNSHA due to triosephosphate isomerase deficiency
Hereditary oculoleptomeningeal amyloid angiopathy
Hereditary optic atrophy
Hereditary orotic aciduria
Hereditary orotic aciduria, type 1
Hereditary orotic aciduria, type 2
Hereditary palmoplantar keratoderma
Hereditary palmoplantar keratoderma Gamborg Nielsen type
Hereditary pancreatitis
Hereditary papillary renal cell carcinoma
Hereditary periodic fever
Hereditary peripheral neuropathy
Hereditary persistence of alpha-fetoprotein
Hereditary persistence of fetal haemoglobin
HPFH A gamma beta^+^ thalassaemia
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia
Hereditary persistence of fetal haemoglobin deletion type
Hereditary persistence of fetal haemoglobin delta beta plus thalassaemia
HPFH linked to beta-globulin gene cluster
Hereditary persistence of fetal haemoglobin thalassaemia
Hereditary persistence of fetal haemoglobin unlinked to beta-globulin gene cluster
Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome
HPFH nondeletion type
Hereditary phaeochromocytoma and paraganglioma
Hereditary platelet function disorder
Hereditary progressive mucinous histiocytosis
Hereditary progressive muscular dystrophy
Hereditary protein C deficiency
Hereditary protein S deficiency
Hereditary pyropoikilocytosis
Hereditary racquet nails
Hereditary red blood cell disorder
Hereditary reticulate melanosis
Hereditary retinal dystrophies in lipidoses
Hereditary retinal dystrophy
Hereditary retinal dystrophy primarily involving retinal pigment epithelium
Hereditary retinal dystrophy primarily involving sensory retina
Hereditary right optic atrophy
Hereditary sclerosing poikiloderma
Hereditary sclerosing poikiloderma of Weary
Hereditary sensorimotor neuropathy with hyperelastic skin
Hereditary sensory and autonomic neuropathy
Hereditary sensory and autonomic neuropathy due to TECPR2 mutation
Hereditary sensory and autonomic neuropathy type 1B
Hereditary sensory and autonomic neuropathy type 7
Hereditary sensory and autonomic neuropathy type I
Hereditary sensory and autonomic neuropathy type II
Hereditary sensory and autonomic neuropathy with deafness and global delay
Hereditary sensory and autonomic neuropathy with spastic paraplegia
Hereditary sensory autonomic neuropathy type IA
Hereditary sensory autonomic neuropathy type IC
Hereditary sensory autonomic neuropathy type ID
Hereditary sensory autonomic neuropathy type IE
Hereditary sensory autonomic neuropathy type IIA
Hereditary sensory autonomic neuropathy type IIB
Hereditary sensory neuropathy
Hereditary site-specific ovarian cancer syndrome
Hereditary skin fragility
Hereditary skin peeling syndrome
Hereditary spastic paraplegia
Hereditary spherocytosis
Hereditary spherocytosis due to beta spectrin defect
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin
Hereditary spherocytosis due to deficiency of protein 4.2
Hereditary spherocytosis due to spectrin deficiency
Hereditary splenic hypoplasia
Hereditary stomatocytosis
Hereditary striate leuconychia
Hereditary thermosensitive neuropathy
Hereditary thrombocytopenia with normal platelets
Hereditary thrombocytopenic disorder
Hereditary thrombophilia
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency
Hereditary thrombophilic dysfibrinogenemia
Hereditary tubulointerstitial disorder
Hereditary vascular fragility
Hereditary vitamin B12 deficiency anaemia
Hereditary vitreoretinopathy
von Willebrand disease type 1
Hereditary von Willebrand disease type IA
von Willebrand disease type IB
von Willebrand disease type IC
von Willebrand disease type 2
Hereditary von Willebrand disease type 2A
Hereditary von Willebrand disease type 2B
Hereditary von Willebrand disease type 2M
von Willebrand disease type 2N
von Willebrand disease type 3
Hereditary white blood cell disorder

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