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32570581000036105: Problem/Diagnosis reference set (foundation metadata concept)


Status: current, Primitive. Date: 31-May 2012. Module: SNOMED Clinical Terms Australian extension

Descriptions:

Id Description Lang Type Status Case? Module
108644681000036112 Problem/Diagnosis reference set (foundation metadata concept) en Fully specified name Active Initial character case insensitive SNOMED Clinical Terms Australian extension
108644691000036114 Problem/Diagnosis reference set en Synonym Active Initial character case insensitive SNOMED Clinical Terms Australian extension
4351251000168110 <p>Supports the recording of a patient problem or diagnosis for medical records within Australia.</p><p>This reference set can be used within implementations of the <em>Medical History DCM</em>&nbsp;(<em>Medical History Detailed Clinical Model Specification.</em> Sydney: NEHTA; 2015. v1.0.).</p><p><b>Target client: </b>This reference set has been developed for those who are implementing the <em>Medical History DCM.</em></p> en Definition Active Case sensitive SNOMED Clinical Terms Australian extension


121309 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Problem/Diagnosis reference set Has licence SNOMED CT-AU licence​ true Inferred relationship Some 1629158626
Problem/Diagnosis reference set Developed by Australian Digital Health Agency true Inferred relationship Some 880198101
Problem/Diagnosis reference set Is a Reference sets for Problem/diagnosis true Inferred relationship Some
Problem/Diagnosis reference set Is a Attribute value type false Inferred relationship Some
Problem/Diagnosis reference set Is a Simple type reference set true Inferred relationship Some

Members
17-ketosteroid in urine specimen above reference range
Increased 17-ketosteroids level
Decreased 17-ketosteroids level
17-ketosteroids within reference range
17p partial trisomy syndrome
17p11.2 microduplication syndrome
17p13.3 microduplication syndrome
17q partial trisomy syndrome
17q11 deletion syndrome
17q11.2 microduplication syndrome
17q12 microdeletion syndrome
17q12 microduplication syndrome
17q21.31 microduplication syndrome
17q23.1-q23.2 duplication syndrome
17q23.1q23.2 microdeletion syndrome
17q24-qter duplication syndrome
17q24.2 microdeletion syndrome
18 month examination abnormal - for observation
18 month examination abnormal - on treatment
18 month examination abnormal - referred
18 month examination normal
18 month examination not attended
18 month examination not wanted
Immunodeficiency associated with 18p syndrome
18p partial monosomy syndrome
18p partial trisomy syndrome
18q partial monosomy syndrome
18q partial trisomy syndrome
19p13.12 microdeletion syndrome
19p13.13 microdeletion syndrome
19p13.3 microduplication syndrome
19q partial trisomy syndrome
19q13.11 microdeletion syndrome
1p partial monosomy
1p21.3 microdeletion syndrome
1p31p32 microdeletion syndrome
1p35.2 microdeletion syndrome
1q partial monosomy
1q21.1 microdeletion
1q21.1 microduplication syndrome
1q41q42 microdeletion syndrome
1q44 microdeletion syndrome
2 level of presenting part in relation to ischial spines
2+ pitting oedema
2,4-Dichlorophenoxyacetic acid poisoning
MCPP poisoning
2-Ketoadipic acidaemia
2-aminoadipic 2-oxoadipic aciduria
2-hydroxyglutaric aciduria
2-methyl-3-hydroxybutyric aciduria
2-methylbutyrylglycinuria
2.5 year examination abnormal - for observation
2.5 year examination abnormal - on treatment
2.5 year examination abnormal - referred
2.5 year examination normal
2.5 year examination not attended
2.5 year examination not wanted
2/60 corrected visual acuity of left eye
2/60 corrected visual acuity of right eye
200 milligram calcium diet
20p partial trisomy syndrome
20p12.2 deletion syndrome
20p12.3 microdeletion syndrome
20p13 microdeletion syndrome
20q partial trisomy
20q11.2 microdeletion syndrome
20q11.2 microduplication syndrome
20q13.33 microdeletion syndrome
21q partial distal trisomy
21q partial monosomy syndrome
21q partial trisomy
21q22.11q22.12 microdeletion syndrome
22q partial monosomy
22q partial trisomy
22q11.2 deletion syndrome
22q11.2 duplication syndrome
22q13.3 deletion syndrome
24 hour support available
24 hour urine volume reduced
24 hour urine volume excessive
24 hour urine volume abnormal
24 hour urine volume normal
2p partial trisomy syndrome
2p13.2 microdeletion syndrome
2p15p16.1 microdeletion syndrome
2p21 microdeletion syndrome
2p21 microdeletion syndrome without cystinuria
2q partial trisomy syndrome
2q23.1 microdeletion syndrome
2q23.1 microduplication syndrome
2q24 microdeletion syndrome
2q31.1 microdeletion syndrome
2q32q33 microdeletion syndrome
2q33.1 microdeletion syndrome
3 beta-Hydroxysteroid dehydrogenase deficiency
3 level of presenting part in relation to ischial spines
3 point swing through gait
3 point swing to gait
3+ pitting oedema
3,3'-diiodothyronine level above reference range
3,3'-diiodothyronine level below reference range

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