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32570171000036103: Situation with explicit context foundation reference set (foundation metadata concept)


Status: current, Primitive. Date: 30-Nov 2009. Module: SNOMED Clinical Terms Australian extension

Descriptions:

Id Description Lang Type Status Case? Module
108642291000036115 Situation with explicit context foundation reference set (foundation metadata concept) en Fully specified name Active Case insensitive SNOMED Clinical Terms Australian extension
108642301000036116 Situation with explicit context foundation reference set en Synonym Active Case insensitive SNOMED Clinical Terms Australian extension
4351371000168114 <p>Supports the recording of clinical context-dependent information in Australian e-health implementations.</p><p>This reference set can be used:<ul><li>Within implementations where use-case specific reference sets for clinical context-dependent information are yet to be developed.</li><li>As the basis for developing further use-case specific reference sets for clinical context-dependent information, through a process of constraint.</li><li>As a benchmark, against which use-case specific reference sets that have been developed by the SNOMED CT-AU user community can be tested, to assure that they are logical constraints of clinical context-dependent content.</li></ul></p><p><b>Target client: </b>NCTS</p> en Definition Active Case sensitive SNOMED Clinical Terms Australian extension


4936 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Situation with explicit context foundation reference set Developed by Australian Digital Health Agency true Inferred relationship Some 555306516
Situation with explicit context foundation reference set Has licence SNOMED CT-AU licence​ true Inferred relationship Some 1304267041
Situation with explicit context foundation reference set Is a Foundation reference sets true Inferred relationship Some
Situation with explicit context foundation reference set Is a Attribute value type false Inferred relationship Some
Situation with explicit context foundation reference set Is a Simple type reference set true Inferred relationship Some

Members
Failed regional anaesthesia
Failed spinal anaesthesia
Failed subcutaneous contraceptive insertion
Failed supraglottic airway ventilation
Failed ureteroscopy
Failed urethrotomy
Failed delivery by vacuum extraction
Fair response to treatment
Fall risk assessment declined
Fall risk care plan declined
Falls advice - hip protectors advised
Falls advice - hip protectors supplied
Family able to participate in care planning
Family attended diabetes structured education programme
Family counselled
Family demonstrates knowledge of disease process
Family distress
Family education about Adverse Childhood Experience questionnaire score
Family education about administration of blood product
Family education about community services
Family education about delirium
Family education about device
Family education about diagnostic test
Family education about dietary regime
Family education about disease
Family education about electrolyte therapy
Family education about fall prevention
Family education about fluid balance
Family education about fluid therapy
Family education about health seeking behaviour
Family education about hygiene
Family education about infant development
Family education about infection prevention
Family education about light therapy
Family education about monitoring respiratory status
Family education about pain management
Family education about prevention of cross infection
Family education about sepsis
Family education about susceptibility to infection
Family education about thermoregulation
Family education about transfer technique
Family education about treatment regime
Family education regarding procedure following death of relative
Family employment circumstance
Family grieving
Family history of Addison disease
Family history of Charcot-Marie-Tooth disease
Family history of Cowden syndrome
Family history of Hashimoto thyroiditis
Family history of Hodgkin's disease
Family history of Marfan syndrome
Family history of Muir-Torré syndrome
Family history of Ménière disease
Family history of Parkinson's disease
Family history of Prader-Willi syndrome
Family history of Raynaud phenomenon
Family history of Rett syndrome
Family history of Steinert myotonic dystrophy
Family history of Tay-Sachs disease
Family history of Turner syndrome
Family history of Von Hippel-Lindau syndrome
Family history of Von Willebrand disease
Family history of abdominal wall defect
Family history of acetylcholinesterase deficiency
Family history of achondroplasia
Family history of acquired immune deficiency syndrome
Family history of acute medical disorder
Family history of alcoholism
Family history of Churg Strauss syndrome
Family history of alpha thalassaemia
Family history of alpha-1-antitrypsin deficiency
Family history of ambiguous genitalia
Family history of amnesia
Family history of amyotrophic lateral sclerosis
Family history of aneurysm of abdominal aorta
Family history of aneurysm of artery
Family history of aneurysm of blood vessel of brain
Family history of aneurysm of thoracic aorta
FH angina female first degree age known
FH angina female first degree age unknown
FH angina male first degree age known
FH angina male first degree age unknown
Family history of anorexia nervosa
Family history of antithrombin III deficiency
Family history of atrial fibrillation
Family history of attention deficit hyperactivity disorder
Family history of attention deficit hyperactivity disorder, predominantly inattentive type
Family history of autism
Family history of autism in sibling
Family history of autosomal aneuploidy
Family history of autosomal translocation
Family history of backache
Family history of bariatric operative procedure
Family history of benign prostatic hyperplasia
Family history of beta thalassaemia
Family history of bilateral hip replacements
Family history of blood coagulation disorder
Family history of BRCA1 gene mutation
Family history of BRCA2 gene mutation
Family history of BRCA gene mutation
Family history of breast cancer gene mutation in first degree relative

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