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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
FH: Anencephaly
FH: Angina
FH: Angina at greater than 60 years
FH: Angina at less than 60 years
Family history: Angina in first degree female relative less than 65 years
FH: Angina in 1st degree male relative <55 years
FH: Ankylosing spondylitis
FH: Anxiety state
FH: Aortic aneurysm
FH: Arthritis
Family history: Asthma
FH: Atherosclerosis
FH: Atopy
FH: Autoimmune disease
FH: Biliary disease
FH: Blindness
FH: Blindness/low vision
FH: Blood disorder
FH: Bowel cancer
FH: Brain disorder
FH: Breast disease
FH: Bronchitis
FH: Bronchus cancer
FH: Brother alive and well
FH: Brother alive with problem
FH: Cardiomyopathy
FH: Cardiovascular disease
Family history: Cataract
Family history: Cerebral palsy
FH: Colitis
FH: Congenital GIT anomaly
FH: Congenital GU anomaly
FH: Congenital heart disease
Family history: Congenital orthopedic anomaly
FH: Consanguinity
FH: Coronary thrombosis
FH: Crohn's disease
FH: Daughter alive and well
FH: Daughter alive with problem
FH: Deafness
FH: Death under 60 years
FH: Depression
FH: Diabetes in pregnancy
FH: Duodenal ulcer
FH: Dyslexia
FH: Ear disorder
FH: Early menarche
Family history: Early menopause
FH: Eczema
FH: Enuresis
FH: Epilepsy
FH: Eye disorder
FH: Father alive and well
FH: Father alive with problem
FH: Father deaf
FH: Female infertility
FH: Fragility fracture
FH: Gallbladder disease
FH: Gastric ulcer
FH: Gastrointestinal disease
FH: Genitourinary disease
FH: Glaucoma
FH: Gonorrhoea
FH: Gout
Family history: Gynaecological problem
FH: Hay fever
FH: Hemiplegia
FH: Haemophilia
FH: Hepatitis
FH: Hereditary spherocytosis
FH: Hip fracture in first degree relative
FH: Hirsutism
Family history: Huntington's chorea
FH: Hypercholesterolaemia
FH: Hypertension
FH: Hypothyroidism
FH: Ischaemic heart disease at greater than 60 years
FH: Ischaemic heart disease at less than 60 years
FH: Late menarche
FH: Late menopause
FH: Liver disease
FH: Longevity
FH: Low vision
FH: Male infertility
Family history: Malignant hyperpyrexia
FH: Manic-depressive state
FH: Maternal hip fracture
FH: Menstrual disorder
Family history: Migraine
FH: Mother alive and well
FH: Mother alive with problem
FH: Motor neurone disease
FH: Multiple pregnancy
FH: Multiple sclerosis
FH: Muscular dystrophy
FH: Musculoskeletal disease
FH: Myocardial infarct in 1st degree male relative <55 years
FH: Myocardial infarction
FH: Myocardial infarction at greater than 60
FH: Myocardial infarction at less than 60
FH: Neoplasm of CNS

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