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32570071000036102: Clinical finding 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
108642091000036110 Clinical finding foundation reference set en Synonym Active Case insensitive SNOMED Clinical Terms Australian extension
108642101000036118 Clinical finding foundation reference set (foundation metadata concept) en Fully specified name Active Case insensitive SNOMED Clinical Terms Australian extension
4350871000168113 <p>Supports the recording of clinical findings and disorders 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 findings and disorders are yet to be developed.</li><li>As the basis for developing further use-case specific reference sets for clinical findings and disorders, 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 content related to clinical finding and disorders.</li></ul></p><p><b>Target client: </b>NCTS</p> en Definition Active Case sensitive SNOMED Clinical Terms Australian extension


115151 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Clinical finding foundation reference set Developed by Australian Digital Health Agency true Inferred relationship Some 1641902964
Clinical finding foundation reference set Has licence SNOMED CT-AU licence​ true Inferred relationship Some 1904103807
Clinical finding foundation reference set Is a Foundation reference sets true Inferred relationship Some
Clinical finding foundation reference set Is a Attribute value type false Inferred relationship Some
Clinical finding foundation reference set Is a Simple type reference set true Inferred relationship Some

Members
Abnormal host response
Abnormal human chorionic gonadotropin
Abnormal human growth hormone
Abnormal illness behaviour
Abnormal immature chorion
Abnormal immature chorionic villi
Abnormal immunological finding in specimen from female genital organ
Abnormal immunological finding in specimen from male genital organ
Abnormal immunological findings in CSF
Abnormal increase in body height
Abnormal increase in number
Abnormal increase in quantity
Abnormal inferior vena caval connection
Abnormal infradian biorhythm
Abnormal innervation syndrome
Abnormal intentional weight loss
Abnormal intercuspation
Abnormal intestinal absorption
Abnormal intraocular pressure
Abnormal intrapericardial course of great arteries
Abnormal involuntary movement
Abnormal jaw closure
Abnormal jaw movement
Abnormal jaw opening
Abnormal jugular venous pressure
Abnormal jugular venous pulse
Abnormal keratinisation
Abnormal keratinisation of hair follicle
Abnormal keratinisation of nail matrix
Abnormal large bowel motility
Abnormal lateral conjugate gaze
Abnormal left ventricular muscle band
Abnormal light reflex at tympanic membrane
Abnormal lipid deposits
Abnormal liver function
Abnormal liver lobulation
Abnormal lung lobation
Abnormal lymphocyte destruction
Abnormal lymphocyte production
Abnormal macromolecular binding
Abnormal macromolecular sequence
ARIA - amyloid-related imaging abnormality
ARIA-E - amyloid-related image abnormality of oedema or effusion
ARIA-H - amyloid-related image abnormality of microhemorrhage or haemosiderosis
Male sexual dysfunction
Abnormal mature chorion
Abnormal megakaryocyte production
Abnormal melanocyte stimulating hormone
Abnormal menstrual cycle
Abnormal metabolic requirement
Abnormal metabolic state due to diabetes mellitus
Abnormal microbiological finding in cerebrospinal fluid
Abnormal microbiological finding in specimen from female genital organ
Abnormal microbiological finding in specimen from male genital organ
Abnormal molecular cross-linking
Abnormal monocyte production
Abnormal monocytes
Abnormal morphology of thoracoabdominal organ
Abnormal motion of ventricular septum
Abnormal motivation
Abnormal movement
Abnormal movement in bone
Abnormal muscle function
Abnormal nasal potential difference
Abnormal nerve conduction
Abnormal nervous system function
Abnormal neurovascular status of distal limb
Abnormal neutrophil production
Nipple abnormality
Abnormal noradrenaline
Abnormal nucleic acid sequence
Abnormal nucleotide base sequence
Abnormal number
Abnormal number of aortic valve cusps
Abnormal number of cusps
Abnormal number of pulmonary valve cusps
Abnormal number of teeth
Abnormal ocular motility
Abnormal optokinetic response
Abnormal organ weight
Abnormal origin of arterial duct
Abnormal origin of left pulmonary artery
Abnormal origin of right pulmonary artery
Abnormal ostium of coronary artery
Abnormal ostium of coronary sinus
Abnormal oxygen supply
Abnormal oxytocin
Abnormal palmar creases
Abnormal pancreatic secretion
Abnormal patient reaction
Abnormal perception
Abnormal pericardiopleural communication
Abnormal perimenopausal bleeding
Abnormal peripheral pulse
Abnormal peripheral vision
Abnormal pitch
Abnormal pituitary follicle stimulating hormone
Abnormal pituitary gonadotropin
Abnormal pituitary luteinising hormone
Abnormal placenta affecting management of mother
Abnormal placental secretion of chorionic gonadotropin

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