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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 operative procedure
Family history of osteogenesis imperfecta
Family history of osteopenia
Family history of osteoporosis
Family history of perinatal disorder
Family history of periodic limb movement disorder
Family history of pernicious anaemia
Family history of phenylketonuria
Family history of polycystic ovary
Family history of polycystic ovary syndrome
Family history of polyp of colon
Family history of pre-eclampsia
Family history of presenile dementia
Family history of problem behaviour
Family history of procedure
Family history of procedure on ovary
Family history of prostate cancer
Family history of protein C deficiency
Family history of protein C resistance
Family history of protein S deficiency
Family history of psoriasis with psoriatic arthritis
Family history of psychotic illness
Family history of pulmonary embolism
Family history of pulmonary emphysema
Family history of pulmonary infundibular stenosis
Family history of radiation therapy
Family history of relative killed
Family history of renal cell carcinoma
Family history of renal failure
Family history of renal stone
Family history of replacement of total knee joint
Family history of restless legs syndrome
Family history of retinal detachment
Family history of retinitis pigmentosa
Family history of rheumatic fever
Family history of sarcoidosis
Family history of scoliosis deformity of spine
Family history of sebaceous adenoma
Family history of sebaceous carcinoma
Family history of seizure disorder
Family history of sex chromosome aneuploidy
Family history of short stature
FH: Sickle cell anaemia
Family history of single congenital anomaly
Family history of sleep apnoea
Family history of smoking
Family history of speech and language disorder
Family history of spinal stenosis
Family history of spinocerebellar ataxia
Family history of Canavan disease
Family history of squamous cell carcinoma of skin
Family history of stenosis of aortic valve
Family history of stroke
Family history of stroke due to aneurysm
Family history of substance abuse
Family history of substance dependency
Family history of sudden cardiac death
Family history of sudden death
FH: Sudden infant death
Family history of syncope
Family history of synovial cyst of popliteal space
Family history of systemic lupus erythematosus
Family history of systemic sclerosis
Family history of tendinous xanthoma in first degree relative
Family history of tendinous xanthoma in second degree relative
Family history of thromboembolic disorder
Family history of tinnitus
Family history of total abdominal hysterectomy with bilateral salpingo-oophorectomy
Family history of transient ischaemic attack
Family history of transplantation of bone marrow
Family history of tremor
Family history of trigeminal neuralgia
Family history of trisomy 13
Family history of trisomy 18
Family history of tuberous sclerosis
Family history of urological disorder
Family history of uveitis
Family history of ventricular premature beats
Family history of visual disturbance
Family history of visual disturbance in childhood
Family history taken
Family history unknown
Family history with explicit context
Family history with explicit context pertaining to aunt
FH: Brother
Family history with explicit context pertaining to daughter
Family history with explicit context pertaining to father
Family history with explicit context pertaining to maternal grandfather
FH: Maternal grandmother
Family history with explicit context pertaining to mother
Family history with explicit context pertaining to paternal grandfather
Family history with explicit context pertaining to paternal grandmother
Family history with explicit context pertaining to sister
Family history with explicit context pertaining to son
Family history with explicit context pertaining to uncle
FH: Age at death
Family history: Allergy
FH: Alopecia
FH: Alzheimer's disease
FH: Anaemia
FH: Anencephaly

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