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

SNOMED CT Concept\SNOMED CT Model Component\Foundation metadata concept\Reference set\...

\Australian reference sets\Reference set by clinical information component\Reference sets for Problem/diagnosis\Problem/Diagnosis reference set

\Simple type reference set\Problem/Diagnosis reference set

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> (<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

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

3,3'-diiodothyronine level below reference range

3,3'-diiodothyronine within reference range

3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency

HMG COA reductase inhibitor adverse reaction

3-Hydroxyisobutyric aciduria

3-Ketoacyl-CoA triolase deficiency

3-Methylglutaconic aciduria

3-Methylglutaconic aciduria type 1

3-Methylglutaconic aciduria type 2

3-Methylglutaconic aciduria type 3

3-Methylglutaconic aciduria type 4

3-Methylglutaconic aciduria with normal 3-methylglutaconyl-CoA hydratase activity

3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency

3-Phosphoglycerate dehydrogenase deficiency

3-methylglutaconic aciduria type 5

3-methylglutaconic aciduria type 7

3-methylglutaconic aciduria type 8

3-methylglutaconic aciduria type 9

3-methylglutaconic aciduria type IV with sensorineural deafness, encephalopathy and Leigh-like syndrome

3-phosphoglycerate dehydrogenase deficiency infantile form

3-phosphoglycerate dehydrogenase deficiency juvenile form

3.5 year examination abnormal - for observation

3.5 year examination abnormal - on treatment

3.5 year examination abnormal - referred

3.5 year examination normal

3.5 year examination not attended

3.5 year examination not wanted

3/60 visual acuity of left eye

3/60 visual acuity of right eye

30 gram fat diet

360 degree sweep of cervix not performed

360 degree sweep of cervix performed

3p partial monosomy syndrome

3p partial trisomy syndrome

3p25.3 deletion syndrome

3q partial trisomy syndrome

3q13 microdeletion syndrome

3q26 microduplication syndrome

3q26q27 microdeletion syndrome

3q27.3 microdeletion syndrome

3q29 microdeletion syndrome

4 level of presenting part in relation to ischial spines

4+ pitting oedema

DNOC causing toxic effect

4-Hydroxyphenylpyruvate dioxygenase deficiency

4-aminopyridine poisoning

4-quinolones adverse reaction

4.5 year examination abnormal - for observation

4.5 year examination abnormal - on treatment

4.5 year examination abnormal - referred

4.5 year examination normal

4.5 year examination not attended

4.5 year examination not wanted

4/60 corrected visual acuity of left eye

4/60 corrected visual acuity of right eye

46 XY disorder of sex development due to maternal ingestion of oestrogen

46,XX androgen-induced disorder of sex development due to maternal adrenal hyperplasia

46,XX androgen-induced disorder of sex development of iatrogenic maternal origin

46,XX disorder of sex development

46,XX disorder of sex development caused by synthetic oral diethylstilbestrol

46,XX disorder of sex development due to synthetic oral progestogen

46,XX disorder of sex development caused by testosterone and/or testosterone derivative

46,XX disorder of sex development due to maternal Krukenberg neoplasm

46,XX disorder of sex development due to maternal adrenal neoplasm

46,XX disorder of sex development due to maternal androluteoma

46,XX disorder of sex development due to maternal arrhenoblastoma

46,XX disorder of sex development with anorectal anomalies syndrome

46,XX disorder of sex development with skeletal anomalies syndrome

46,XX ovarian dysgenesis, short stature syndrome

46,XX ovotesticular disorder of sex development

46,XX testicular disorder of sex development

46,XY disorder of sex development

46,XY disorder of sex development due to environmental chemical exposure

46,XY disorder of sex development due to isolated 17,20-lyase deficiency

46,XY disorder of sex development due to maternal ingestion of progestogen

46,XY disorder of sex development, adrenal insufficiency due to CYP11A1 deficiency

46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome

46,XY ovotesticular disorder of sex development

46,XY partial gonadal dysgenesis

48,XYYY syndrome

49,XXXYY syndrome

49,XYYYY syndrome

4H leucodystrophy

4p partial monosomy syndrome

4p partial trisomy syndrome

4p16.3 microduplication syndrome

4q partial monosomy syndrome

4q partial trisomy syndrome

4q21 microdeletion syndrome

4q25 proximal deletion syndrome

5 level of presenting part in relation to ischial spines

5,10-Methylenetetrahydrofolate reductase deficiency

5-HT3-receptor antagonist adverse reaction

5-HT3-receptor antagonist overdose

5-HT3-receptor antagonist poisoning

5-Oxoprolinase deficiency

5-amino-4-imidazole carboxamide ribosiduria

5-aminosalicylic acid adverse reaction

5-aminosalicylic acid overdose

5-aminosalicylic acid poisoning

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