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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 malposition of gallbladder
Congenital malposition of heart
Congenital malposition of humerus
Congenital malposition of ilium
Congenital malposition of inferior vena cava
Congenital malposition of innominate artery
Congenital malposition of intestinal tract
Congenital malposition of ischium
Congenital malposition of kidney
Congenital malposition of liver
Congenital malposition of lumbar vertebra
Congenital malposition of lung
Congenital malposition of metacarpal bone
Congenital malposition of metatarsal bone
Congenital malposition of nares
Congenital malposition of nasal septum
Congenital malposition of nasal turbinate
Congenital malposition of nose
Congenital malposition of ovary
Congenital malposition of palate rugae
Congenital malposition of pinna
Congenital malposition of pubis
Congenital malposition of pulmonary artery
Congenital malposition of radius
Congenital malposition of rib
Congenital malposition of sacral vertebra
Congenital malposition of spleen
Congenital malposition of sternebra
Congenital malposition of subclavian artery
Congenital malposition of superior vena cava
Congenital malposition of talus
Congenital malposition of tarsal bone
Congenital malposition of testis
Congenital malposition of the thyroid gland
Congenital malposition of thoracic vertebra
Congenital malposition of thymus
Congenital malposition of tibia
Congenital malposition of trachea
Congenital malposition of ulna
Congenital malposition of vas deferens
Congenital malrotation of duodenum
Congenital malrotation of heart
Congenital malrotation of intestine
Congenital malrotation of limb
Congenital mandibular asymmetry
Congenital mandibular hyperplasia
Congenital mass of mitral leaflet
Congenital maxillary asymmetry
Congenital maxillary hyperplasia
Congenital maxillary hypoplasia
Congenital megaduodenum
Congenital megalogastria
Congenital melanocytic naevus of face
Congenital melanocytic naevus of trunk
Congenital melanosis
Congenital melanosis of sclera
Congenital membranous cataract
Congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunisation
Congenital meningocele
Congenital mesenteroaxial volvulus of stomach
Congenital mesocolic hernia
Congenital metatarsus valgus
Congenital methaemoglobinaema with defective methaemoglobin-reducing system
Congenital methaemoglobinaemia
Congenital methaemoglobinaemia with abnormal methaemoglobins
Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome
Congenital microcheilia
Congenital microgastria
Congenital microgastria with limb reduction defect syndrome
Congenital micrognathism
Congenital microhepatia
Congenital microvillous atrophy
Congenital midvalvar ring of mitral leaflet
Congenital miosis
Congenital misalignment of arch of cervical vertebra
Congenital misalignment of arch of lumbar vertebra
Congenital misalignment of arch of sacral vertebra
Congenital misalignment of arch of thoracic vertebra
Congenital misalignment of centrum of cervical vertebra
Congenital misalignment of centrum of lumbar vertebra
Congenital misalignment of centrum of sacral vertebra
Congenital misalignment of centrum of thoracic vertebra
Congenital misalignment of palate rugae
Congenital misalignment of pubis
Congenital misalignment of rib
Congenital misalignment of sternebra
Congenital mixed conductive and sensorineural hearing loss
Congenital monosaccharide malabsorption
Congenital myopathy Paradas type
Congenital muscular dystrophy due to LMNA mutation
Congenital muscular dystrophy type 1A
Congenital muscular dystrophy type 1B
Congenital muscular dystrophy with arthrogryposis multiplex congenita
Congenital muscular dystrophy with cerebellar involvement
Congenital muscular dystrophy with hyperlaxity
Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome
Congenital muscular dystrophy with integrin alpha-7 deficiency
Congenital muscular dystrophy with intellectual disability
Congenital muscular dystrophy with intellectual disability and severe epilepsy
Congenital muscular dystrophy without intellectual disability
Congenital muscular hypertrophy-cerebral syndrome

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