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32570381000036103: Cardiovascular finding 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
108643201000036118 Cardiovascular finding reference set (foundation metadata concept) en Fully specified name Active Case insensitive SNOMED Clinical Terms Australian extension
108643211000036116 Cardiovascular finding reference set en Synonym Active Case insensitive SNOMED Clinical Terms Australian extension
4350841000168118 <p>Supports the recording of cardiovascular findings in Australian e-health implementations. This reference set has been developed from the <em>Clinical finding foundation reference set</em>.</p><p>This reference set can be used:<ul><li>Within implementations where use-case specific reference sets for cardiovascular findings are yet to be developed.</li><li>As the basis for developing further use-case specific reference sets for cardiovascular findings 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 relating to cardiovascular findings.</li></ul></p><p><b>Target client: </b>Australian e-health clinical information systems, for example, in Cardiology.</p> en Definition Active Case sensitive SNOMED Clinical Terms Australian extension


8360 members. Search Members:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cardiovascular finding reference set Has licence SNOMED CT-AU licence​ true Inferred relationship Some 492615774
Cardiovascular finding reference set Developed by Australian Digital Health Agency true Inferred relationship Some 1241576299
Cardiovascular finding reference set Is a Clinical finding foundation reference set false Inferred relationship Some
Cardiovascular finding reference set Is a Cardiology clinical group true Inferred relationship Some
Cardiovascular finding reference set Is a Attribute value type false Inferred relationship Some
Cardiovascular finding reference set Is a Simple type reference set true Inferred relationship Some

Members
Heart sounds exaggerated
Heart sounds normal
Heart transplant failure and rejection
Heart valve calcification
Heart valve disease
Heart valve regurgitation
Heart valve stenosis
Heart valve stenosis and regurgitation
Heart-hand syndrome Slovenian type
Heart-hand syndrome type 2
Heart-hand syndrome type 3
Heart-lung transplant failure and rejection
Haemangioma of choroid
Haemangioma of intracranial structure
Haemangioma of left choroid
Haemangioma of liver
Haemangioma of right choroid
Haemangioma of skin
Haemangioma of skin in pregnancy
Haemangiopericytoma
Haematoma of cord
Hemicardia
Hemicrania continua
Hemiplegic migraine
Hemispheric retinal vein occlusion
Haemodialysis-associated hypotension
Haemodynamic instability
Haemodynamically insignificant ventricular septal defect
Haemodynamically stable
HELLP syndrome
Haemopericardium
Haemopericardium due to and following acute myocardial infarction
Haemorrhage associated with renal dialysis graft
Hemorrhage of blood vessel
Haemorrhage of colon due to angiodysplasia of colon
Haemorrhage of transplant artery
Haemorrhage of transplanted vein
Haemorrhagic gastroenteritis
Haemorrhagic gastropathy
Haemorrhagic mucosa of stomach
Haemorrhagic rubella
Haemorrhagic smallpox
Haemorrhoids
Haemorrhoids in pregnancy
Haemorrhoids in pregnancy and puerperium
Haemorrhoids in puerperium
Haemorrhoids without complication
Heparin-induced thrombocytopenia with thrombosis
Hepatic artery embolism
Hepatic artery thrombosis
Hepatic infarction
Hepatic portal vein tumour invasion
Hepatic vein thrombosis
Hepatic vein to coronary sinus
Hepatic vein to left atrium and right atrium
Hepatic vein to left sided atrium
Hepatic vein to right sided atrium
Hepatic veno-occlusive disease with immunodeficiency syndrome
Hepatojugular reflux
Hepatoportal microvascular dysplasia
Hepatoportal sclerosis
Hepatopulmonary syndrome
Hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome
Hereditary arterial and articular multiple calcification syndrome
Hereditary benign telangiectasia
Hereditary cavernous haemangioma of brain
Hereditary cerebral amyloid angiopathy, Dutch type
Hereditary cerebral amyloid angiopathy, Icelandic type
Hereditary cerebral haemorrhage with amyloidosis
Hereditary cerebrovascular amyloidosis
Hereditary cutaneous vascular syndrome
Hereditary diffuse endocapillary proliferative glomerulonephritis
Hereditary dysplasia of blood vessel
Hereditary haemorrhagic telangiectasia of gingiva
Hereditary neurocutaneous angiomata
Hereditary vascular fragility
Heritable pulmonary arterial hypertension
Heritable pulmonary arterial hypertension due to ALK1 or endoglin mutation
Heritable pulmonary arterial hypertension due to BMPR2 mutation
Hibernating myocardium
High altitude pulmonary hypertension
High degree second degree atrioventricular block
High output heart failure
High risk of heart failure, stage B
High ventilation-perfusion ratio
High-renin essential hypertension
His bundle tachycardia
Histiocytic vasculitis of skin
Histiocytoid mitochondrial cardiomyopathy
Histiocytoid mitochondrial cardiomyopathy due to cytochrome aa3 deficiency
Histoplasma capsulatum with endocarditis
Histoplasma capsulatum with pericarditis
Histoplasma duboisii with endocarditis
Histoplasma duboisii with pericarditis
Histoplasmosis syndrome of bilateral eyes
Histoplasmosis syndrome of left eye
Histoplasmosis syndrome of right eye
Histoplasmosis with pericarditis
Holoacardius acephalus
Holoacardius acormus
Holoacardius amorphus

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Reference Sets

Australian dialect reference set

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