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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
X-ray of thumb abnormal
X-ray of thumb normal
X-ray of tibia abnormal
X-ray of tibia normal
X-ray of tibia/fibula abnormal
X-ray of tibia/fibula normal
X-ray pelvimetry abnormal
X-ray pelvimetry normal
X-ray phalanges of fingers abnormal
X-ray phalanges of fingers normal
X-ray shoulder/arm abnormal
X-ray shoulder/arm normal
X-ray thoracic cage abnormal
X-ray thoracic cage normal
XK aprosencephaly syndrome
XS2 phenotype
XX males
XXXXY syndrome
XXXY syndrome
XXYY syndrome
XY females
XY type gonadal dysgenesis with associated anomalies syndrome
XY, female phenotype
X^o^rX^o^r blood group phenotype
Xamoterol adverse reaction
Xanthelasma
Increased xanthine
Xanthine adverse reaction
Xanthine and/or xanthine derivative overdose
Decreased xanthine
Xanthine overdose
Xanthine oxidase inhibitor adverse reaction
Xanthine within reference range
Xanthinuria
Xanthium species poisoning
Xanthogranuloma
Xanthogranuloma of choroid plexus
Xanthogranulomatous cholecystitis
Xanthomatous hypophysitis
Xanthogranulomatous pyelonephritis
Xanthogranulomatous salpingitis
Xanthoma diabeticorum
Xanthoma disseminatum
Xanthoma due to abnormality of lipid metabolism
Xanthoma due to lipid storage disease
Xanthoma due to primary chylomicronaemia
Xanthoma due to primary combined hyperlipidaemia
Xanthoma due to primary hypercholesterolaemia
Xanthoma due to primary hypertriglyceridaemia
Xanthoma due to secondary hyperlipidaemia
Xanthoma of bilateral eyelids
Bilateral xanthoma of lower eyelids
Xanthoma of bilateral upper eyelids
Xanthoma of bone
Xanthoma of eyelid
Xanthoma of left eyelid
Xanthoma of left lower eyelid
Xanthoma of left upper eyelid
Xanthoma of lower eyelid
Xanthoma of lung
Xanthoma of right eyelid
Xanthoma of right lower eyelid
Xanthoma of right upper eyelid
Xanthoma of upper eyelid
Xanthoma planum of eyelid
Xanthoma secondary to lymphoedema
Xanthoma tendinosum
Xanthomatosis
Palmar xanthoma
Xanthomatosis, familial
Xanthopsia
Xanthorrhoea species poisoning
Xanthurenic aciduria
Xenophobia
Xerocytosis
Xeroderma
Xeroderma in genetic syndrome
Xeroderma of eyelid
Xeroderma of left eyelid
Xeroderma of left upper eyelid
Xeroderma of lower eyelid
Xeroderma of right eyelid
Xeroderma of right upper eyelid
Xeroderma of upper eyelid
Xeroderma pigmentosum
Xeroderma pigmentosum and Cockayne syndrome complex
Xeroderma pigmentosum, group A
Xeroderma pigmentosum, group B
Xeroderma pigmentosum, group C
Xeroderma pigmentosum, group D
Xeroderma pigmentosum, group E
Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group G
Xeroderma pigmentosum, variant form
XTE syndrome
Xerophthalmia
Xerosis due to atopic dermatitis
Bilateral corneal xerosis
Aptyalism
Xerostomia caused by ionising radiation
Xerostomia due to autoimmune disease

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