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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
Yellow colour
Yellow colour of faeces
Yellow fever
Yellow fever suspected
Yellow fever vaccination contraindicated
Yellow fever vaccination given
Yellow mutant oculocutaneous albinism
Yellow nails
Yellow or jaundiced colour
Yellow skin
Yellow sputum
Yellow vaginal discharge
Yellowish red colour
Yersinia enterocolitica food poisoning
Yersinia enterocolitica or Yersinia frederiksenii or Yersinia intermedia
Yersinia erythema nodosum
Yersinia frederiksenii or Yersinia intermedia
Yersinia not isolated
Yersiniosis
Yin deficiency
Yin excess
Yolk sac absent
Yolk sac present
Yolk sac tumour
Yolk sac tumour of central nervous system
Young adult-onset distal hereditary motor neuropathy
Young offender
Young onset Parkinson's disease
Young's syndrome
Yunis-Varon dysplasia
Yus type
Z deformity of thumb
Zalcitabine adverse reaction
Zamia species poisoning
Zanamivir resistant virus present
Zar
Zebra body myopathy
Zechi Ceide syndrome
Zellweger syndrome
Zellweger's-like syndrome
Zellweger-like syndrome without peroxisomal anomaly
Zidovudine adverse reaction
Zieria arborescens poisoning
Zieve's syndrome
Zika virus disease
Zimmermann-Laband syndrome
Zinc adverse reaction
Zinc deficiency
Zinc depletion syndrome
Zinc excess
Abnormal zinc level in blood
Zinc phosphide poisoning
Zinc poisoning
Zinc salt poisoning
Zinc sulfide poisoning
Zinc-responsive dermatosis
Ziprkowski-Margolis syndrome
Zirconium granuloma of skin
Zirconium pneumoconiosis
Zollinger-Ellison syndrome
Zolpidem adverse reaction
Zolpidem overdose
Zolpidem poisoning
Zonal bullous emphysema
Zonular dehiscence
Zonular dialysis
Zonular disruption
Zonular laxity
Zonular nonsenile cataract
Zonular traction peripheral retinal tuft
Zoonotic form of cutaneous leishmaniasis
Zoophobia
Zopiclone adverse reaction
Zopiclone overdose
Zopiclone poisoning
Zoster sine herpete
Zosteriform lentiginosis
Zosteriform lichen planus
Zosteriform reticulate hyperpigmentation
Zuclopenthixol adverse reaction
Zuclopenthixol decanoate adverse reaction
Zuclopenthixol decanoate overdose
Zuclopenthixol decanoate poisoning
Zuclopenthixol poisoning
Zygadenus species poisoning
Zygomycosis
^A^gamma delta beta^0^ thalassaemia
a and b waves reduced
beta^+^ Thalassaemia, normal Hb A>2<, type 2
cDE haplotype
cDe haplotype
cdE haplotype
cde haplotype
de Barsy syndrome
i>1< phenotype
i>2< phenotype
i>adult< phenotype
i>cord< phenotype
k+ phenotype
k- phenotype
NDE1-related microhydranencephaly

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