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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 Reference Sets
108642091000036110 Clinical finding foundation reference set en Synonym Active Case insensitive SNOMED Clinical Terms Australian extension Australian dialect reference set: Preferred
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

111112 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
-1 level of presenting part in relation to ischial spines
-2 level of presenting part in relation to ischial spines
-3 level of presenting part in relation to ischial spines
-4 level of presenting part in relation to ischial spines
-5 level of presenting part in relation to ischial spines
0 level of presenting part in relation to ischial spines
0-5 mitoses per 10 HPF (score = 1)
1 level of presenting part in relation to ischial spines
1 o'clock position on mammogram
1 or more mitotic figure per mm2
1 to 12 seizures a year
1 to 7 seizures a week
1 year examination abnormal - for observation
1 year examination abnormal - on treatment
1 year examination abnormal - referred
1+ pitting oedema
MPTP-induced parkinsonism
1/60 corrected visual acuity of left eye
1/60 corrected visual acuity of right eye
10 day examination abnormal - for observation
10 day examination abnormal - on treatment
10 day examination abnormal - referred
10 o'clock position on mammogram
10 or more mitotic figures per 10 high power field
10 year examination abnormal - for observation
10 year examination abnormal - on treatment
10 year examination abnormal - referred
10 year examination normal
10-20 mitoses per 10 HPF (score = 2)
10g monofilament sensation L foot abnormal
10g monofilament sensation L foot normal
10g monofilament sensation R foot abnormal
10g monofilament sensation R foot normal
10g monofilament sensation absent
10g monofilament sensation present
10p partial monosomy syndrome
10p partial trisomy syndrome
10q partial monosomy syndrome
10q partial trisomy syndrome
10q22.3q23.3 microdeletion syndrome
10q22.3q23.3 microduplication syndrome
11 o'clock position on mammogram
11p partial monosomy syndrome
11p partial trisomy syndrome
11p15 deletion syndrome
11p15 duplication syndrome
11p15.4 microduplication syndrome
11q partial monosomy syndrome
11q partial trisomy syndrome
12 o'clock position on mammogram
12p partial monosomy syndrome
12p partial trisomy syndrome
12p12.1 microdeletion syndrome
12q partial trisomy syndrome
12q14 microdeletion syndrome
12q15 deletion syndrome
12q15q21.1 microdeletion syndrome
12q24.31-q24.32 deletion syndrome
13p partial trisomy syndrome
13q partial monosomy syndrome
13q partial trisomy syndrome
13q12.3 microdeletion syndrome
14q partial distal trisomy syndrome
14q partial proximal trisomy syndrome
14q partial trisomy syndrome
14q11.2 microdeletion syndrome
14q11.2 microduplication syndrome
14q12 microdeletion syndrome
14q22q23 microdeletion syndrome
14q24.1q24.3 microdeletion syndrome
14q32 deletion syndrome
15 year examination abnormal - for observation
15 year examination abnormal - on treatment
15 year examination abnormal - referred
15 year examination normal
150 milligram calcium diet
15q overgrowth syndrome
15q partial monosomy syndrome
15q partial trisomy syndrome
15q11.2 microdeletion syndrome
15q11q13 microduplication syndrome
15q13.3 microduplication syndrome
15q14 microdeletion syndrome
16p partial trisomy syndrome
16p11.2p12.2 microdeletion syndrome
16p11.2p12.2 microduplication syndrome
16p12.2 microdeletion syndrome
16p13.11 microdeletion syndrome
16p13.11 microduplication syndrome
16p13.3 microduplication syndrome
16q partial monosomy syndrome
16q partial trisomy syndrome
16q24.1 microdeletion syndrome
16q24.3 microdeletion syndrome
17 alpha-Hydroxyprogesterone aldolase deficiency
17-ketosteroid in urine specimen above reference range
17p partial trisomy syndrome
17p11.2 microduplication syndrome
17p13.3 microduplication syndrome
17q partial trisomy syndrome
17q11 deletion syndrome

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