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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
Family history of breast cancer gene mutation in first degree relative
FH: Bronchitis/COPD
Family history of bulimia nervosa
FH: Butyrylcholinesterase deficiency
Family history of cancer
Family history of cancer of colon
Family history of cancer of the oesophagus
Family history of cardiac arrhythmia
FH: cardiac disorder
Family history of cardiovascular disease in first degree female relative less than 65 years of age
Family history of cardiovascular disease in first degree male relative less than 55 years of age
Family history of carotid endarterectomy
Family history of coeliac disease
FH: CNS disorder
Family history of cerebral artery occlusion
Family history of cerebral infarction
Family history of cholecystectomy
Family history of chromosomal anomaly
Family history of chronic medical disorder
Family history of chronic myeloid leukaemia
FH: COPD
Family history of chronic renal impairment
Family history of chronic respiratory disease
Family history of chronic ulcerative proctitis
Family history of cleft lip
Family history of cleft palate
Family history of cleft palate with cleft lip
Family history of clinical finding
Family history of clubfoot
Family history of colour blindness
Family history of colorectal cancer
Family history of combined hyperlipidaemia
Family history of complete trisomy 21 syndrome
Family history of complex congenital heart disease
Family history of conduction disorder of the heart
Family history of congenital anomaly of cardiovascular system
Family history of congenital cataract
Family history of congenital disease
Family history of developmental hip dysplasia
Family history of congenital hydrocephalus
Family history of congenital immunodeficiency disease
Family history of congenital microcephaly
FH: Congenital RS anomaly
Family history of congestive heart failure
Family history of connective tissue disorder
Family history of coronary arteriosclerosis
Family history of craniosynostosis
FH: Cystic fibrosis
Family history of cystic hygroma
Family history of death due to natural cause
Family history of death of unknown cause
Family history of degenerative disorder of macula
Family history of dementia
Family history of development disorder
FH: Diabetes mellitus
FH: Diabetes mellitus in first degree relative
Family history of type 1 diabetes mellitus
Family history of type 2 diabetes mellitus
Family history of diabetes mellitus with complication
Family history of disability
Family history of disorder
Family history of disorder of immune function
Family history of disorder of lung
Family history of disorder of pancreas
Family history of disorder of peripheral nervous system
Family history of disorder of vein
Family history of dissection of aorta
Family history of diverticulitis of colon
Family history of double heterozygous familial hypercholesterolaemia
Family history of eating disorder
FH: Oedema of lower limb
Family history of endocarditis
Family history of endocrine disorders
Family history of eruptive xanthoma
Family history of familial dysautonomia
Family history of familial hypercholesterolaemia
Family history of familial multiple polyposis syndrome
Family history of female genital tract disorder
Family history of fracture of proximal end of femur
Family history of fragile X syndrome
Family history of galactosaemia
Family history of gene mutation
Family history of genetic disorder carrier
Family history of genetic mutation for Lynch syndrome
Family history of glycogen storage disease
Family history of headache disorder
Family history of hearing loss
Family history of hearing loss in childhood
Family history of heart failure
Family history of helminth infection
Family history of haematuria
Family history of haemochromatosis
Family history of haemoglobinopathy
Family history of haemoglobinopathy E
Family history of hereditary disease
Family history of hereditary nonpolyposis colon cancer
Family history of heritable malignancy
Family history of HIV
Family history of hydronephrosis
Family history of hyperbetalipoproteinaemia
FH: Hypercholesterolaemia in first degree relative

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