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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
5-aminosalicylic acid poisoning
5-HT secreting neuroendocrine tumour
5/60 corrected visual acuity of left eye
5/60 corrected visual acuity of right eye
50 gram fat diet
5p partial monosomy syndrome
5p13 microduplication syndrome
5q14.3 microdeletion syndrome
5q22.2 deletion syndrome
5q31.3 microdeletion syndrome
5q35 microduplication syndrome
6 week examination abnormal - for observation
6 week examination abnormal - on treatment
6 week examination abnormal - referred
6-10 mitoses per 10 HPF (score = 2)
6-Pyruvoyl-tetrahydrobiopterin synthase deficiency
6/12 pinhole visual acuity of left eye
6/12 pinhole visual acuity of right eye
6/12 visual acuity of left eye
6/12 visual acuity of right eye
6/15 visual acuity of left eye
6/15 visual acuity of right eye
6/18 pinhole visual acuity of left eye
6/18 pinhole visual acuity of right eye
6/18 visual acuity of left eye
6/18 visual acuity of right eye
6/24 pinhole visual acuity of left eye
6/24 pinhole visual acuity of right eye
6/24 visual acuity of left eye
6/24 visual acuity of right eye
6/3 corrected visual acuity of left eye
6/3 corrected visual acuity of right eye
6/36 pinhole visual acuity of left eye
6/36 pinhole visual acuity of right eye
6/36 visual acuity of left eye
6/36 visual acuity of right eye
6/4 visual acuity of left eye
6/4 visual acuity of right eye
6/48 visual acuity of left eye
6/48 visual acuity of right eye
6/5 pinhole visual acuity of left eye
6/5 pinhole visual acuity of right eye
6/5 visual acuity of left eye
6/5 visual acuity of right eye
6/6 pinhole visual acuity of left eye
6/6 pinhole visual acuity of right eye
6/6 visual acuity of left eye
6/6 visual acuity of right eye
6/60 pinhole visual acuity of left eye
6/60 pinhole visual acuity of right eye
6/60 visual acuity of left eye
6/60 visual acuity of right eye
6/7.5 visual acuity of left eye
6/7.5 visual acuity of right eye
6/9 pinhole visual acuity of left eye
6/9 pinhole visual acuity of right eye
6/9 visual acuity of left eye
6/9 visual acuity of right eye
60 to 80 percent of predicted peak expiratory flow rate
6p partial trisomy syndrome
6p22 microdeletion syndrome
6q partial trisomy syndrome
6q terminal deletion syndrome
6q16 microdeletion syndrome
6q25 microdeletion syndrome
70 gram fat diet
7p partial monosomy
7p partial trisomy
7p12-p14 deletion syndrome
7p21.1 deletion syndrome
7p22.1 microduplication syndrome
7q partial monosomy
7q partial trisomy
7q11.23 microduplication syndrome
7q31 microdeletion syndrome
8 month examination abnormal - for observation
8 month examination abnormal - on treatment
8 month examination abnormal - referred
8 week examination abnormal - for observation
8 week examination abnormal - on treatment
8 week examination abnormal - referred
8-9 month exam normal
8-9 month exam not attended
8-9 month exam not wanted
8-9 month examination abnormal - for observation
8-9 month examination abnormal - on treatment
8-9 month examination abnormal - referred
8p inverted duplication deletion syndrome
8p partial monosomy syndrome
8p11.2 deletion syndrome
8p23.1 duplication syndrome
8p23.1 microdeletion syndrome
8q partial monosomy syndrome
8q partial trisomy syndrome
8q12 microduplication syndrome
8q13 microdeletion syndrome
8q21.11 microdeletion syndrome
8q22.1 microdeletion syndrome
8q24.3 microdeletion syndrome
9p partial trisomy syndrome
9p13 microdeletion syndrome

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